Jump to content

Trifluoromethylation

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Citation bot (talk | contribs) at 02:51, 26 October 2023 (Removed proxy/dead URL that duplicated identifier. | Use this bot. Report bugs. | #UCB_CommandLine). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Trifluoromethylation in organic chemistry describes any organic reaction that introduces a trifluoromethyl group in an organic compound.[1][2][3][4] Trifluoromethylated compounds are of some importance in pharmaceutical industry and agrochemicals. Several notable pharmaceutical compounds have a trifluoromethyl group incorporated: fluoxetine, mefloquine, Leflunomide, nulitamide, dutasteride, bicalutamide, aprepitant, celecoxib, fipronil, fluazinam, penthiopyrad, picoxystrobin, fluridone, norflurazon, sorafenib and triflurazin. A relevant agrochemical is trifluralin. The development of synthetic methods for adding trifluoromethyl groups to chemical compounds is actively pursued in academic research.

History

The first to investigate trifluoromethyl groups in relationship to biological activity was F. Lehmann in 1927.[5] An early review appeared in 1958.[6] An early synthetic method was developed by Frédéric Swarts in 1892,[7] based on antimony fluoride. In this reaction benzotrichloride was reacted with SbF3 to form PhCF2Cl and PhCF3. In the 1930s Kinetic Chemicals and IG Farben replaced SbF3 with HF. The McLoughlin-Thrower reaction (1968) is an early coupling reaction using iodofluoroalkanes, iodoaromatic compounds and copper.[8] In 1969 Kobayashi & Kumadaki adapted their protocol for trifluoromethylations.[9][10]

McLoughlin-Thrower reaction
McLoughlin-Thrower reaction (1968)

Reagents

Trifluoromethyltrimethylsilane

Preparation of the trifluoromethyltrimethylsilane was reported by Ingo Ruppert in 1984.[11] In 1989, Prakash and Olah first reported activation of TMSCF3 by fluoride to perform nucleophilic trifluoromethylation of carbonyl compounds.[12] In the same year, Stahly described similar reactions for the synthesis of trifluoromethylated phenols and anilines.[13] Since then TMSCF3 has been widely used as a nucleophilic trifluoromethylating agent.[14][15]

An example is the trifluoromethylation of cyclohexanone in THF using tetrabutylammonium fluoride.[16]

Cyclohexanol trifluoromethylation
Trifluoromethylation using

trifluoromethyltrimethylsilane[16]

The substrates can be aryl halides.[17][18] Potassium (trifluoromethyl)trimethoxyborate for this purpose has been synthesised from B(OMe)3, CF3SiMe3 and KF.[19] Aryl functionalization by C-H activation has also been reported.[20][21]

Sodium trifluoroacetate

Sodium trifluoroacetate as a reagent for trifluoromethylations was introduced by Matsui in 1981. In the original scope the substrate was an aromatic halide and the metal salt copper(I)iodide.[22][23]

Trifluoromethane

Fluoroform (CF3H) has been employed as a trifluoromethylation reagent for aldehydes in combination with a strong base.[24]

Trifluoromethylation fluoroform folleas 1998
Trifluoromethylation fluoroform folleas 1998[24]

Trifluoroiodomethane

Trifluoroiodomethane is a reagent in aromatic coupling reactions. It has also been used with enones, for example with chalcone, a reaction catalysed by diethyl zinc and Wilkinson's catalyst:[25]

Trifluoromethylation trifluoroiodomethane
Trifluoromethylation using diethyl zinc and Wilkinson's catalyst[25]

Trifluoromethyl sulfone

Trifluoromethyl sulfone (PhSO2CF3) and trifluoromethyl sulfoxide (PhSOCF3) can be used for trifluoromethylations of electrophiles[26]

Trifluoromethanesulfonyl chloride

Trifluoromethanesulfonyl chloride (or triflyl chloride, CF3SO2Cl) can be used in a highly efficient method to introduce a trifluoromethyl group to aromatic and heteroaromatic systems, including known pharmaceuticals such as Lipitor. The chemistry is general and mild, and uses a photoredox catalyst and a light source at room temperature.[27]

Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis

Sodium trifluoromethanesulfinate

Sodium trifluoromethanesulfinate (CF3SO2Na) as a trifluoromethylation reagent was introduced by Langlois in 1991.[28] The reaction requires t-butyl hydroperoxide and generally a metal and proceeds through a radical mechanism. The reagent has been applied with heterocyclic substrates[29]

Trifluorination Langlois reagent 2011
Trifluorination Langlois reagent 2011[29]

Umemoto reagents

Umemoto reagents are (trifluoromethyl)dibenzoheterocyclic salts, such as 5-(trifluoromethyl)dibenzothiophenium triflate and 5-(trifluoromethyl)dibenzothiophenium tetrafluoroborate.[30][31]

Trifluoromethyl-metal reagents

Many CF3-containing metal complexes have been prepared, and some are useful for trifluoromethylation. The most obvious reagent is CF3Li, which can be generated by lithium-iodide exchange. This compound is however unstable even at low temperatures. It degrades to lithium fluoride and difluorocarbene. Trifluoromethyl copper(I) reagents are more useful. These reagents are generated in situ by reaction of CF3I with copper powder in polar solvents.[32] Hg(CF3)2, prepared by decarboxylation of the trifluoroacetate, has proven useful for the trifluoromethylation of other metals.[33]

Reaction types

Aromatic coupling reactions

In coupling reactions between aromatic compounds and metal-trifluoromethyl complexes the metal is usually copper, Pd and Ni are less prominent.[1] The reactions are stoichiometric or catalytic. In the McLoughlin-Thrower reaction (1962) iodobenzene reacts with trifluoroiodomethane (CF3I) and copper powder in dimethylformamide at 150 °C to trifluoromethylbenzene. The intermediate in this reaction type is a perfluoromethyl-metal complex.

A palladium acetate catalysed reaction described in 1982 used zinc powder with the main intermediate believed to be CF3ZnI with Pd(0) is the active catalyst.[34][35] The first copper catalysed coupling was reported in 2009 and based on an iodoarene, a trifluoromethylsilane, copper iodide and 1,10-phenanthroline.[36] Variations include another CF3 donor potassium (trifluoromethyl)trimethoxyborate,[37] the use of aryl boronic acids[38][39] or the use of a trifluoromethyl sulfonium salt[40] or the use of a trifluoromethylcopper(I) phenanthroline complex.[41] A catalytic palladium catalysed reaction was reported in 2010 using aryl halides, (trifluoromethyl)triethylsilane and allylpalladium chloride dimer[42]

Aromatic trifluoromethylation Kitazume 1982 Aromatic trifluoromethylation Oishi 2009
Aromatic trifluoromethylation Kitazume 1982[34] Aromatic catalytic

trifluoromethylation Oishi 2009[36]

Radical trifluoromethylation

In radical trifluoromethylation the active species is the trifluoromethyl free radical.[43] Reagents such as bromotrifluoromethane and haloform have been used for this purpose[44][45][46] but in response to the Montreal Protocol alternatives such as trifluoroiodomethane have been developed as replacement.[47][48] One particular combination is CF3I / triethylborane[49][50] Other reagents that generate the CF3 radical are sodium trifluoromethanesulfinate and bis(trifluoroacetyl) peroxide.

Trifluorododecanone synthesis 1991
Trifluoromethylation using CF3I and triethylborane.

The base is 2,6-lutidine[49]

In the CF3 radical the fluorine atom is an electron-withdrawing group via the inductive effect but also a weak pi donor through interaction of the fluorine lone pair with the radical center's SOMO. Compared to the methyl radical the CF3 radical is pyramidal (angle 107.8 °C ) with a large inversion barrier, electrophilic and also more reactive. In reaction with styrene it is 440 times more reactive.[51] An early report (1949) describes the photochemical reaction of iodotrifluoromethane with ethylene to 3-iodo-1,1,1-trifluoropropane.[52] Reagents that have been reported for the direct trifluoromethylation of arenes are CF3I, CF3Br (thermal or photochemical), silver trifluoroacetate/TiO2 (photochemical) and sodium trifluoromethanesulfinate/Cu(OSO2CF3)2/tBuOOH.

Nucleophilic trifluoromethylation

In nucleophilic trifluoromethylation the active species is the CF3− anion.[53] It was, however, widely believed that the trifluoromethyl anion is a transient species and thus cannot be isolated or observed in the condensed phase. Contrary to the popular belief, the CF3 anion, with [K(18-crown-6)]+ as a countercation, was produced and characterized by Prakash and coworkers.[54] The challenges associated with observation of CF3 anion are alluded to its strong basic nature and its tendency to form pentacoordinated silicon species, such as [Me3Si(CF3)2]− or [Me3Si(F)(CF3)]−.

The reactivity of fluoroform in combination with a strong base such as t-BuOK with carbonyl compounds in DMF is an example.[53] Here CF3− and DMF form an hemiaminolate adduct ([Me2NCH(O)CF3]K).[24][55][56][57]

Trifluoromethylation methyl fluorosulfonyldifluoroacetate
trifluoromethylation using methyl fluorosulfonyldifluoroacetate.

The intermediate is CF3Cu[58]

Electrophilic trifluoromethylation

In electrophilic trifluoromethylation the active trifluoromethyl donor group carries a positive charge.[59][60] Production of an CF3+ cation has been described as "extremely hard" [61] The first relevant reagent, a diaryl(trifluoromethyl) sulfonium salt (Ar2S+CF3SbF6−) was developed in 1984 by reaction of an aryltrifluoromethyl sulfoxide 1 with SF3+SbF6− followed by reaction with an electron-rich arene.[62] The reagent was used in trifluoromethylation of a thiophenolate. S-(trifluoromethyl)dibenzothiophenium tetrafluoroborate is a commercially available and known trifluoromethylation reagent based on the same principle first documented in 1990.[63][64] In this type of compound sulfur has been replaced by oxygen, selenium and tellurium. Examples of substrates that have been investigated are pyridine, aniline, triphenylphosphine and the lithium salt of phenylacetylene.

Electrophilic Perfluoroalkylating Agents
5-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate 5-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole
5-(Trifluoromethyl)dibenzothiophenium
trifluoromethanesulfonate 		5-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole

Another group of trifluoromethyl donors are hypervalent iodine(III)[65]–CF3 reagents for example 3,3-dimethyl-1-(trifluoromethyl)-1,2-benziodoxole.[66][67][68][69] Some of these are known as Togni reagents, such as Togni reagent II. Substrates are thiols, alcohols, phosphines, (hetero) arenes,[70] unactivated olefins[71] and unsaturated carboxylic acids.[72]

Togni reagent synth of ethyl-(R)-2-amino-3-(trifluoromethylthio)propanoate hydrochloride
Trifluoromethylation at a thiol group using hypervalent iodine [70]

The reaction mechanism of electrophilic trifluoromethylations has been described as controversial with polar substitution or single electron transfer as likely candidates.[61]

Asymmetric trifluoromethylation

In asymmetric trifluoromethylation the trifluoromethyl group is added to the substrate in an enantioselective way.[73][74] Ruppert's reagent has been used for this purpose in an asymmetric induction approach to functionalise chiral amino acid derivates,[75] saccharides,[76] and steroids. Because Ruppert's reagent requires a tetraalkylammonium fluoride, chiral ammonium fluorides have been employed in asymmetric catalysis.[77][78] In the field of electrophilic trifluoromethylation an early contribution involved reaction of a metal enolate with a trifluoromethyl chalcogen salt in presence of a chiral boron catalyst.[79]

Asymmetic trifluorination Iseki 1994 Asymmetic trifluorination Caron 2003
Asymmetric trifluoromethylation Iseki 1994[77] Asymmetric trifluormethylation Caron 2003[78]

More recent examples of highly enantioselective methods for the α-trifluoromethylation of carbonyls are available through enamine catalysis of aldehydes (photoredox[80] or iodonium[81]), copper catalysis of β-ketoesters,[82] and radical addition to zirconium enolates.[83]

References

  1. ^ a b Tomashenko, O. A.; Grushin, V. V. (2011). "Aromatic Trifluoromethylation with Metal Complexes". Chemical Reviews. 111 (8): 4475–4521. doi:10.1021/cr1004293. PMID 21456523.
  2. ^ Furuya, T.; Kamlet, A. S.; Ritter, T. (2011). "Catalysis for fluorination and trifluoromethylation". Nature. 473 (7348): 470–477. Bibcode:2011Natur.473..470F. doi:10.1038/nature10108. PMC 3119199. PMID 21614074.
  3. ^ Besset, T.; Schneider, C. D.; Cahard, D. (2012). "Tamed Arene and Heteroarene Trifluoromethylation". Angewandte Chemie International Edition. 51 (21): 5048–5050. doi:10.1002/anie.201201012. PMID 22488902.
  4. ^ Alonso, C. N.; Martínez De Marigorta, E.; Rubiales, G.; Palacios, F. (2015). "Carbon Trifluoromethylation Reactions of Hydrocarbon Derivatives and Heteroarenes". Chemical Reviews. 115 (4): 1847–1935. doi:10.1021/cr500368h. PMID 25635524.
  5. ^ Lehmann, F. "Chemical constitution and activity. Aromatic fluorine compounds." Arch. exp. Pathol. Pharmakol 130 (1928): 250-255.
  6. ^ Yale, H. L. (1959). "The Trifluoromethyl Group in Medical Chemistry". Journal of Medicinal and Pharmaceutical Chemistry. 1 (2): 121–133. doi:10.1021/jm50003a001. PMID 13665284.
  7. ^ Swarts (1892). Acad. Roy. Belg. 3 (24): 474. {{cite journal}}: Missing or empty |title= (help)
  8. ^ McLoughlin, V. C. R.; Thrower, J. (1969). "A route to fluoroalkyl-substituted aromatic compounds involving fluoroalkylcopper intermediates". Tetrahedron. 25 (24): 5921–5940. doi:10.1016/S0040-4020(01)83100-8.
  9. ^ Kobayashi, Y.; Kumadaki, I. (1969). "Trifluoromethylation of aromatic compounds". Tetrahedron Letters. 10 (47): 4095–4096. doi:10.1016/S0040-4039(01)88624-X.
  10. ^ Folléas, B. ̂T.; Marek, I.; Normant, J. F.; Saint-Jalmes, L. (2000). "Fluoroform: An Efficient Precursor for the Trifluoromethylation of Aldehydes". Tetrahedron. 56 (2): 275–283. doi:10.1016/S0040-4020(99)00951-5.
  11. ^ Ruppert, Ingo; Schlich, Klaus; Volbach, Wolfgang (January 1984). "Die ersten CF3-substituierten organyl(chlor)silane". Tetrahedron Letters. 25 (21): 2195–2198. doi:10.1016/S0040-4039(01)80208-2.
  12. ^ Prakash, G. K. Surya; Krishnamurti, Ramesh; Olah, George A. (January 1989). "Synthetic methods and reactions. 141. Fluoride-induced trifluoromethylation of carbonyl compounds with trifluoromethyltrimethylsilane (TMS-CF3). A trifluoromethide equivalent". Journal of the American Chemical Society. 111 (1): 393–395. doi:10.1021/ja00183a073.
  13. ^ Stahly, G. Patrick; Bell, Donald R. (June 1989). "A new method for synthesis of trifluoromethyl-substituted phenols and anilines". The Journal of Organic Chemistry. 54 (12): 2873–2877. doi:10.1021/jo00273a020.
  14. ^ G. K. Surya Prakash; Andrei K. Yudin (1997). "Perfluoroalkylation with Organosilicon Reagents". Chemical Reviews. 97 (3): 757–786. doi:10.1021/cr9408991. PMID 11848888.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  15. ^ Xiao Liu, Cong Xu, Mang Wang, and Qun Liu (2015). "Trifluoromethyltrimethylsilane: Nucleophilic Trifluoromethylation and Beyond". Chemical Reviews. 115 (2): 683–730. doi:10.1021/cr400473a. PMID 24754488.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  16. ^ a b Ramaiah, Pichika; Krishnamurti, Ramesh; K. Surya Prakash, G. (1995). "1-TRIFLUOROMETHYL-1-CYCLOHEXANOL". Organic Syntheses. 72 (72): 232. doi:10.15227/orgsyn.072.0232.
  17. ^ Morimoto, H.; Tsubogo, T.; Litvinas, N. D.; Hartwig, J. F. (2011). "A Broadly Applicable Copper Reagent for Trifluoromethylations and Perfluoroalkylations of Aryl Iodides and Bromides". Angewandte Chemie. 123 (16): 3877–3882. Bibcode:2011AngCh.123.3877M. doi:10.1002/ange.201100633. PMC 3159489. PMID 21442711.
  18. ^ Oishi, Masahiro; Kondo, Hideaki; Amii, Hideki (2009). "Aromatic trifluoromethylation catalytic in copper". Chemical Communications. 2009 (14): 1909–1911. doi:10.1039/B823249K. PMID 19319442.
  19. ^ Knauber, T.; Arikan, F.; Röschenthaler, G.-V.; Gooßen, L. J. (2011). "Copper-Catalyzed Trifluoromethylation of Aryl Iodides with Potassium (Trifluoromethyl)trimethoxyborate". Chemistry: A European Journal. 17 (9): 2689–2697. doi:10.1002/chem.201002749. PMID 21274956.
  20. ^ Ye, Yingda; Lee, Shin Hee; Sanford, Melanie S. (2011). "Silver-Mediated Trifluoromethylation of Arenes Using TMSCF3". Organic Letters. 13 (20): 5464–5467. doi:10.1021/ol202174a. PMC 3229100. PMID 21932827.
  21. ^ Hafner, A.; Bräse, S. (2012). "Ortho-Trifluoromethylation of Functionalized Aromatic Triazenes". Angewandte Chemie International Edition. 51 (15): 3713–3715. doi:10.1002/anie.201107414. PMID 22318969.
  22. ^ Matsui, Kiyohide; Tobita, Etsuko; Ando, Midori; Kondo, Kiyosi (1981). "A convenient trifluoromethylation of aromatic halides with sodium trifluoroacetate". Chemistry Letters. 10 (12): 1719–1720. doi:10.1246/cl.1981.1719.
  23. ^ Langlois, Bernard R.; Roques, Nicolas (October 2007). "Nucleophilic trifluoromethylation of aryl halides with methyl trifluoroacetate". Journal of Fluorine Chemistry. 128 (10): 1318–1325. doi:10.1016/j.jfluchem.2007.08.001.
  24. ^ a b c Folléas, Benoît; Marek, Ilan; Normant, Jean-F; Jalmes, Laurent Saint (May 1998). "Fluoroform: an efficient precursor for the trifluoromethylation of aldehydes". Tetrahedron Letters. 39 (19): 2973–2976. doi:10.1016/S0040-4039(98)00391-8.
  25. ^ a b Sato, Kazuyuki; Omote, Masaaki; Ando, Akira; Kumadaki, Itsumaro (2006). "TRIFLUOROMETHYLATION AT THE a-POSITION OF b,b-UNSATURATED KETONES: 4-PHENYL-3-(TRIFLUOROMETHYL)BUTAN-2-ONE". Organic Syntheses. 83 (83): 177. doi:10.15227/orgsyn.083.0177.
  26. ^ Prakash, G. K. Surya; Hu, Jinbo; Olah, George A. (September 2003). "Alkoxide- and Hydroxide-Induced Nucleophilic Trifluoromethylation Using Trifluoromethyl Sulfone or Sulfoxide". Organic Letters. 5 (18): 3253–3256. doi:10.1021/ol035045u. PMID 12943400.
  27. ^ Nagib, David A.; MacMillan, David W. C. (8 December 2011). "Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis". Nature. 480 (7376): 224–228. Bibcode:2011Natur.480..224N. doi:10.1038/nature10647. PMC 3310175. PMID 22158245.
  28. ^ Langlois, Bernard R.; Laurent, Eliane; Roidot, Nathalie (December 1991). "Trifluoromethylation of aromatic compounds with sodium trifluoromethanesulfinate under oxidative conditions". Tetrahedron Letters. 32 (51): 7525–7528. doi:10.1016/0040-4039(91)80524-A.
  29. ^ a b Ji, Y.; Brueckl, T.; Baxter, R. D.; Fujiwara, Y.; Seiple, I. B.; Su, S.; Blackmond, D. G.; Baran, P. S. (15 August 2011). "Innate C-H trifluoromethylation of heterocycles". Proceedings of the National Academy of Sciences. 108 (35): 14411–14415. Bibcode:2011PNAS..10814411J. doi:10.1073/pnas.1109059108. PMC 3167544. PMID 21844378.
  30. ^ Zhang, Cai (11 July 2014). "Recent advances in trifluoromethylation of organic compounds using Umemoto's reagents". Organic & Biomolecular Chemistry. 12 (34): 6580–9. doi:10.1039/C4OB00671B. PMID 25011917.
  31. ^ Li, Huiqin (3 September 2012). "Umemoto's Reagent". Synlett. 23 (15): 2289–2290. doi:10.1055/s-0032-1317176.
  32. ^ Donald J. Burton, Long Lu "Fluorinated Organometallic Compounds" Topics in Current Chemistry, 1997, Vol. 193, p. 45.
  33. ^ Reint Eujen "Bis(Trifluoromethyl)Mercury" 1986, volume 24, p. 52. doi:10.1002/9780470132555.ch16
  34. ^ a b Kitazume, Tomoya; Ishikawa, Nobuo (1982). "Palladium-Catalyzed Cross-Coupling Reactions Between Allyl, Vinyl or Aryl Halide and Perfluoroalkyl Iodide with Zinc and Ultrasonic Irradiation". Chemistry Letters. 11 (1): 137–140. doi:10.1246/cl.1982.137.
  35. ^ Kitazume, Tomoya; Ishikawa, Nobuo (1985). "Ultrasound-promoted selective perfluoroalkylation on the desired position of organic molecules". Journal of the American Chemical Society. 107 (18): 5186–5191. doi:10.1021/ja00304a026.
  36. ^ a b Oishi, M.; Kondo, H.; Amii, H. (2009). "Aromatic trifluoromethylation catalytic in copper". Chem. Commun. 2009 (14): 1909–1911. doi:10.1039/B823249K. PMID 19319442.
  37. ^ Knauber, T.; Arikan, F.; Roschenthaler, G.-V.; Gooßen, L. J. (2011). "Copper-catalyzed trifluoromethylation of aryl iodides with potassium (trifluoromethyl) trimethoxyborate". Chem. Eur. J. 17 (9): 2689–2697. doi:10.1002/chem.201002749. PMID 21274956.
  38. ^ Chu, L.; Qing, F.-L. (2010). "Copper-mediated oxidative trifluoromethylation of boronic acids". Org. Lett. 12 (21): 5060–5063. doi:10.1021/ol1023135. PMID 20923196.
  39. ^ Senecal, Todd D.; Parsons, Andrew T.; Buchwald, Stephen L. (18 February 2011). "Room Temperature Aryl Trifluoromethylation via Copper-Mediated Oxidative Cross-Coupling". The Journal of Organic Chemistry. 76 (4): 1174–1176. doi:10.1021/jo1023377. PMC 3093444. PMID 21235259.
  40. ^ Cheng-, Cheng-Pan; Zhang, Pan; Wang, Ling; et al. (2011). "Copper-mediated trifluoromethylation of heteroaromatic compounds by trifluoromethyl sulfonium salts". Angew. Chem. Int. Ed. 50 (8): 1896–1900. doi:10.1002/anie.201006823. PMID 21328665.
  41. ^ Morimoto, H.; Tsubogo, T.; Litvinas, N. D.; Hartwig, J. F. (2011). "A broadly applicable copper reagent for trifluoromethylations and perfluoroalkylations of aryl iodides and bromides". Angew. Chem. Int. Ed. 50 (16): 3793–3798. doi:10.1002/anie.201100633. PMC 3159489. PMID 21442711.
  42. ^ Cho, E. J.; Senecal, T. D.; Kinzel, T.; Zhang, Y.; Watson, D. A.; Buchwald, S. L. (24 June 2010). "The Palladium-Catalyzed Trifluoromethylation of Aryl Chlorides". Science. 328 (5986): 1679–1681. Bibcode:2010Sci...328.1679C. doi:10.1126/science.1190524. PMC 3005208. PMID 20576888.
  43. ^ Ma, Jun-An; Cahard, Dominique (September 2007). "Strategies for nucleophilic, electrophilic, and radical trifluoromethylations". Journal of Fluorine Chemistry. 128 (9): 975–996. doi:10.1016/j.jfluchem.2007.04.026.
  44. ^ Andrieux, Claude P.; Gelis, Laurence; Saveant, Jean-Michel (January 1989). "Unusual reactions resulting from the addition on olefins of trifluoromethyl radicals obtained from dissociative electron transfer between electrochemically generated aromatic anion radicals and trifluoromethyl bromide". Tetrahedron Letters. 30 (37): 4961–4964. doi:10.1016/S0040-4039(01)80554-2.
  45. ^ Uneyama, Kenji; Kitagawa, Kouichi; Kitagawa, Kouichi (January 1991). "Perfluoroalkyl-selenation of olefins". Tetrahedron Letters. 32 (3): 375–378. doi:10.1016/S0040-4039(00)92632-7.
  46. ^ Uneyama, Kenji; Kanai, Masatomi (December 1991). "Generation of perfluoroalkyl radicals at low temperature by tellurolate mediated electron transfer". Tetrahedron Letters. 32 (50): 7425–7426. doi:10.1016/0040-4039(91)80124-O.
  47. ^ Rasmusson, Gary H.; Brown, Ronald D.; Arth, Glen E. (March 1975). "Photocatalyzed reaction of trifluoromethyl iodide with steroidal dienones". The Journal of Organic Chemistry. 40 (6): 672–675. doi:10.1021/jo00894a002. PMID 1133630.
  48. ^ Lan-Hargest, Hsuan-Yin; Elliott, John D.; Eggleston, Drake S.; Metcalf, Brian W. (January 1987). "The photochemical rearrangement of a steroidal dienol triflate". Tetrahedron Letters. 28 (52): 6557–6560. doi:10.1016/S0040-4039(00)96912-0.
  49. ^ a b Miura, Katsukiyo; Takeyama, Yoshihiro; Oshima, Koichiro; Utimoto, Kiitiro (1991). "Triethylborane Induced Perfluoroalkylation of Silyl Enol Ethers and Ketene Silyl Acetals with Perfluoroalkyl Iodides". Bulletin of the Chemical Society of Japan. 64 (5): 1542–1553. doi:10.1246/bcsj.64.1542.
  50. ^ Miura, Katsukiyo; Taniguchi, Masahiko; Nozaki, Kyoko; Oshima, Koichiro; Utimoto, Kiitiro (January 1990). "Triethylborane induced perfluoroalkylation of silyl enol ethers or germyl enol ethers with perfluoroalkyl iodides". Tetrahedron Letters. 31 (44): 6391–6394. doi:10.1016/S0040-4039(00)97073-4.
  51. ^ Studer, Armido (3 September 2012). "A "Renaissance" in Radical Trifluoromethylation". Angewandte Chemie International Edition. 51 (36): 8950–8958. doi:10.1002/anie.201202624. PMID 22890985.
  52. ^ Haszeldine, R. N. (1949). "603. The reactions of fluorocarbon radicals. Part I. The reaction of iodotrifluoromethane with ethylene and tetrafluoroethylene". Journal of the Chemical Society (Resumed): 2856. doi:10.1039/JR9490002856.
  53. ^ a b Langlois, Bernard R.; Billard, Thierry; Roussel, Solveig (February 2005). "Nucleophilic trifluoromethylation". Journal of Fluorine Chemistry. 126 (2): 173–179. doi:10.1016/j.jfluchem.2004.11.007.
  54. ^ Prof. Dr. G. K. Surya Prakash, Dr. Fang Wang, Zhe Zhang, Prof. Dr. Ralf Haiges, Dr. Martin Rahm, Prof. Dr. Karl O. Christe, Dr. Thomas Mathew, Prof. Dr. George A. Olah (2014). "Long-Lived Trifluoromethanide Anion: A Key Intermediate in Nucleophilic Trifluoromethylations". Angew. Chem. Int. Ed. 53 (43): 11575–11578. doi:10.1002/anie.201406505. PMID 25146595.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  55. ^ Shono, Tatsuya; Ishifune, Manabu; Okada, Toshio; Kashimura, Shigenori (January 1991). "Electroorganic chemistry. 130. A novel trifluoromethylation of aldehydes and ketones promoted by an electrogenerated base". The Journal of Organic Chemistry. 56 (1): 2–4. doi:10.1021/jo00001a002.
  56. ^ Barhdadi, Rachid; Troupel, Michel; Périchon, Jacques (1998). "Coupling of fluoroform with aldehydes using an electrogenerated base". Chemical Communications (12): 1251–1252. doi:10.1039/A801406J.
  57. ^ Large, Sylvie; Roques, Nicolas; Langlois, Bernard R. (December 2000). "Nucleophilic Trifluoromethylation of Carbonyl Compounds and Disulfides with Trifluoromethane and Silicon-Containing Bases". The Journal of Organic Chemistry. 65 (26): 8848–8856. doi:10.1021/jo000150s. PMID 11149825.
  58. ^ Fei, Xiang-Shu; Tian, Wei-Sheng; Ding, Kai; Wang, Yun; Qing-Yun, Chen (2010). "New, Convenient Route for Trifluoromethylation of Steroidal Molecules". Org. Synth. 87 (87): 126. doi:10.15227/orgsyn.087.0126.
  59. ^ Shibata, N.; Matsnev, A.; Cahard, D. (2010). "Shelf-stable electrophilic trifluoromethylating reagents: A brief historical perspective". Beilstein Journal of Organic Chemistry. 6: 65. doi:10.3762/bjoc.6.65. PMC 2919266. PMID 20703379.
  60. ^ Umemoto, T. (1996). "Electrophilic Perfluoroalkylating Agents". Chemical Reviews. 96 (5): 1757–1778. doi:10.1021/cr941149u. PMID 11848810.
  61. ^ a b Barata-Vallejo, S. N.; Lantaño, B.; Postigo, A. (2014). "Recent Advances in Trifluoromethylation Reactions with Electrophilic Trifluoromethylating Reagents". Chemistry: A European Journal. 20 (51): 16806–16829. doi:10.1002/chem.201404005. hdl:11336/30347. PMID 25335765.
  62. ^ Yagupolskii, L. M.; Kondratenko, N. V.; Timofeeva, G. N. J. Org. Chem. USSR 1984, 20, 103–106.
  63. ^ Teruo, U.; Sumi, I. (1990). "Power-variable trifluoromethylating agents, (trifluoromethyl)dibenzothio- and -selenophenium salt system". Tetrahedron Letters. 31 (25): 3579–3582. doi:10.1016/S0040-4039(00)94447-2.
  64. ^ Umemoto, T.; Ishihara, S. (1993). "Power-variable electrophilic trifluoromethylating agents. S-, Se-, and Te-(trifluoromethyl)dibenzothio-, -seleno-, and -tellurophenium salt system". Journal of the American Chemical Society. 115 (6): 2156–2164. doi:10.1021/ja00059a009.
  65. ^ Here, iodine is considered to be less electronegative (2.3) than carbon (2.5), per the IUPAC definition that de facto mandates that Allen electronegativity be used; the more commonly encountered Pauling electronegativity scale would imply that the molecule in question would be that of iodine(I), not iodine(III).
  66. ^ Eisenberger, P.; Gischig, S.; Togni, A. (2006). "Novel 10-I-3 Hypervalent Iodine-Based Compounds for Electrophilic Trifluoromethylation". Chemistry: A European Journal. 12 (9): 2579–2586. doi:10.1002/chem.200501052. PMID 16402401.
  67. ^ Kieltsch, I.; Eisenberger, P.; Togni, A. (2007). "Mild Electrophilic Trifluoromethylation of Carbon- and Sulfur-Centered Nucleophiles by a Hypervalent Iodine(III)–CF3 Reagent". Angewandte Chemie International Edition. 46 (5): 754–757. doi:10.1002/anie.200603497. PMID 17154193.
  68. ^ Eisenberger, P.; Kieltsch, I.; Armanino, N.; Togni, A. (2008). "Mild electrophilic trifluoromethylation of secondary and primary aryl- and alkylphosphines using hypervalent iodine(iii)–CF3 reagents". Chemical Communications (13): 1575–7. doi:10.1039/B801424H. PMID 18354804. S2CID 205709340.
  69. ^ Stanek, K.; Koller, R.; Togni, A. (2008). "Reactivity of a 10-I-3 Hypervalent Iodine Trifluoromethylation Reagent with Phenols". The Journal of Organic Chemistry. 73 (19): 7678–7685. doi:10.1021/jo8014825. PMID 18771328.
  70. ^ a b "Preparation of a Trifluoromethyl Transfer Agent: 1-Trifluoromethyl-1,3-Dihydro-3,3-Dimethyl-1,2-Benziodoxole". Organic Syntheses. 88: 168. 2011. doi:10.15227/orgsyn.088.0168.
  71. ^ Parsons, A. T.; Buchwald, S. L. (2011). "Copper-Catalyzed Trifluoromethylation of Unactivated Olefins". Angewandte Chemie International Edition. 50 (39): 9120–9123. doi:10.1002/anie.201104053. PMC 3390945. PMID 21919144.
  72. ^ He, Z.; Luo, T.; Hu, M.; Cao, Y.; Hu, J. (2012). "Copper-Catalyzed Di- and Trifluoromethylation of α,β-Unsaturated Carboxylic Acids: A Protocol for Vinylic Fluoroalkylations". Angewandte Chemie International Edition. 51 (16): 3944–3947. doi:10.1002/anie.201200140. PMID 22407851.
  73. ^ Ma, Jun-An; Cahard, Dominique (December 2004). "Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions". Chemical Reviews. 104 (12): 6119–6146. doi:10.1021/cr030143e. PMID 15584697.
  74. ^ Lin, Jin-Hong; Xiao, Ji-Chang (November 2014). "Recent advances in asymmetric fluorination and fluoroalkylation reactions via organocatalysis". Tetrahedron Letters. 55 (45): 6147–6155. doi:10.1016/j.tetlet.2014.09.031.
  75. ^ Skiles, Jerry W.; Fuchs, Victor; Miao, Clara; Sorcek, Ronald; Grozinger, Karl G.; Mauldin, Scott C.; Vitous, Jana; Mui, Philip W.; Jacober, Stephen (February 1992). "Inhibition of human leukocyte elastase (HLE) by N-substituted peptidyl trifluoromethyl ketones". Journal of Medicinal Chemistry. 35 (4): 641–662. doi:10.1021/jm00082a005. PMID 1542092.
  76. ^ Bansal, Romesh C.; Dean, Barbara; Hakomori, Sen-itiroh; Toyokuni, Tatsushi (1991). "Synthesis of trifluoromethyl analogue of L-fucose and 6-deoxy-D-altrose". Journal of the Chemical Society, Chemical Communications (12): 796. doi:10.1039/C39910000796.
  77. ^ a b Iseki, Katsuhiko; Nagai, Takabumi; Kobayashi, Yoshiro (May 1994). "Asymmetric trifluoromethylation of aldehydes and ketones with trifluoromethyltrimethylsilane catalyzed by chiral quaternary ammonium fluorides". Tetrahedron Letters. 35 (19): 3137–3138. doi:10.1016/S0040-4039(00)76850-X.
  78. ^ a b Caron, Stéphane; Do, Nga; Arpin, Patrice; Larivée, Alexandre (August 2003). "Enantioselective Addition of a Trifluoromethyl Anion to Aryl Ketones and Aldehydes". Synthesis. 2003 (11): 1693–1698. doi:10.1055/s-2003-40889.
  79. ^ Umemoto, Teruo; Adachi, Kenji (September 1994). "New Method for Trifluoromethylation of Enolate Anions and Applications to Regio-, Diastereo- and Enantioselective Trifluoromethylation". The Journal of Organic Chemistry. 59 (19): 5692–5699. doi:10.1021/jo00098a030.
  80. ^ Nagib, David A.; Scott, Mark E.; MacMillan, David W. C. (2009). "Enantioselective α-Trifluoromethylation of Aldehydes via Photoredox Organocatalysis". Journal of the American Chemical Society. 131 (31): 10875–10877. doi:10.1021/ja9053338. PMC 3310169. PMID 19722670.
  81. ^ Allen, Anna E.; MacMillan, David W. C. (2010). "The Productive Merger of Iodonium Salts and Organocatalysis: A Non-photolytic Approach to the Enantioselective α-Trifluoromethylation of Aldehydes". Journal of the American Chemical Society. 132 (14): 4986–4987. doi:10.1021/ja100748y. PMC 2880471. PMID 20297822.
  82. ^ Deng, Qing-Hai; Wadepohl, Hubert; Gade, Lutz H. (2012). "Highly Enantioselective Copper-Catalyzed Electrophilic Trifluoromethylation of β-Ketoesters". Journal of the American Chemical Society. 134 (26): 10769–10772. doi:10.1021/ja3039773. PMID 22693950.
  83. ^ Herrmann, Aaron T.; Smith, Lindsay L.; Zakarian, Armen (2012). "A Simple Method for Asymmetric Trifluoromethylation of-Acyl Oxazolidinones via Ru-Catalyzed Radical Addition to Zirconium Enolates". Journal of the American Chemical Society. 134 (16): 6976–6979. doi:10.1021/ja302552e. PMC 3375393. PMID 22486383.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Trifluoromethylation&oldid=1181933232"