User talk:Mglutamate

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Mglutamate, you are invited to the Teahouse![edit]

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Hi Mglutamate! Thanks for contributing to Wikipedia.
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16:06, 27 February 2017 (UTC)

Welcome, but be careful[edit]

Welcome to Wikipedia. Here are suggested readings: WP:SECONDARY and WP:COI. The gist of these guidelines are:

  • Wikipedia prefers citations to reviews and books, not primary journal references (tens of thousands appear annually). Citing secondary sources is the encyclopedic style.
  • Do not cite yourself or your colleagues. It's called conflict of interest. Many new editors cite themselves mainly. That behavior is inappropriate, not to mention in bad taste. Below are a collection of the citations that you have added. There seems to be a trend. You might revisit these edits since you might not have understood the guidelines here.

If you have questions, many editors can offer advice. Happy editing.--Smokefoot (talk) 03:11, 9 April 2018 (UTC)[reply]

[1][2][3][4]Cite error: A <ref> tag is missing the closing </ref> (see the help page). [5][6][7] [8][9][10][11][12][13][14]

  1. ^ Stoermer, Martin J.; Wickramasinghe, Wasantha A.; Byriel, Karl A.; Hockless, David C. R.; Skelton, Brian W.; Sobolev, Alexandre N.; White, Allan H.; Mak, Jeffrey Y. W.; Fairlie, David P. (2017-12-08). "Stereoelectronic Effects on Dienophile Separation Influence the Diels-Alder Synthesis of Molecular Clefts". European Journal of Organic Chemistry. 2017 (45): 6793–6796. doi:10.1002/ejoc.201701319. ISSN 1099-0690.
  2. ^ Martin, David; Kehrli, Stefan; d'Augustin, Magali; Clavier, Hervé; Mauduit, Marc; Alexakis, Alexandre (2006-07-01). "Copper-Catalyzed Asymmetric Conjugate Addition of Grignard Reagents to Trisubstituted Enones. Construction of All-Carbon Quaternary Chiral Centers". Journal of the American Chemical Society. 128 (26): 8416–8417. doi:10.1021/ja0629920. ISSN 0002-7863.
  3. ^ Mak, Jeffrey Y. W.; Williams, Craig M. (2011-11-30). "Enantioselective total synthesis of (−)-neovibsanin G and (−)-14-epi-neovibsanin G". Chem. Commun. 48 (2): 287–289. doi:10.1039/c1cc15995j. ISSN 1364-548X.
  4. ^ Mak, Jeffrey Y. W.; Williams, Craig M. (2012-04-01). "Total Synthesis of (-)-Neovibsanin G and (-)-14-epi-Neovibsanin G: Towards the Synthesis of 15-O-Methylneovibsanin F and 14-epi-15-O-Methylneovibsanin F". European Journal of Organic Chemistry. 2012 (10): 2001–2012. doi:10.1002/ejoc.201101796. ISSN 1099-0690.
  5. ^ Corbett, Alexandra J.; Eckle, Sidonia B. G.; Birkinshaw, Richard W.; Liu, Ligong; Patel, Onisha; Mahony, Jennifer; Chen, Zhenjun; Reantragoon, Rangsima; Meehan, Bronwyn. "T-cell activation by transitory neo-antigens derived from distinct microbial pathways". Nature. 509 (7500): 361–365. doi:10.1038/nature13160.
  6. ^ Cite error: The named reference :4 was invoked but never defined (see the help page).
  7. ^ Kjer-Nielsen, Lars; Patel, Onisha; Corbett, Alexandra J.; Nours, Jérôme Le; Meehan, Bronwyn; Liu, Ligong; Bhati, Mugdha; Chen, Zhenjun; Kostenko, Lyudmila. "MR1 presents microbial vitamin B metabolites to MAIT cells". Nature. doi:10.1038/nature11605.
  8. ^ Bredt, J.; Houben, Jos.; Levy, Paul (1902-04-01). "Ueber isomere Dehydrocamphersäuren, Lauronolsäuren und Bihydrolauro-Lactone". Berichte der deutschen chemischen Gesellschaft. 35 (2): 1286–1292. doi:10.1002/cber.19020350215. ISSN 1099-0682.
  9. ^ Mak, Jeffrey Y. W.; Pouwer, Rebecca H.; Williams, Craig M. (2014-12-08). "Natural Products with Anti-Bredt and Bridgehead Double Bonds". Angewandte Chemie International Edition. 53 (50): 13664–13688. doi:10.1002/anie.201400932. ISSN 1521-3773.
  10. ^ Mak, Jeffrey Y. W.; Pouwer, Rebecca H.; Williams, Craig M. (2014-12-08). "Natural Products with Anti-Bredt and Bridgehead Double Bonds". Angewandte Chemie International Edition. 53 (50): 13664–13688. doi:10.1002/anie.201400932. ISSN 1521-3773.
  11. ^ Corbett, Alexandra J.; Eckle, Sidonia B. G.; Birkinshaw, Richard W.; Liu, Ligong; Patel, Onisha; Mahony, Jennifer; Chen, Zhenjun; Reantragoon, Rangsima; Meehan, Bronwyn. "T-cell activation by transitory neo-antigens derived from distinct microbial pathways". Nature. 509 (7500): 361–365. doi:10.1038/nature13160.
  12. ^ Mak, Jeffrey Y. W.; Xu, Weijun; Fairlie, David P. (2015-01-01). Thiazoles in Peptides and Peptidomimetics. Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg. pp. 1–32. doi:10.1007/7081_2015_176.
  13. ^ Mak, Jeffrey Y. W.; Xu, Weijun; Fairlie, David P. (2015-01-01). Thiazoles in Peptides and Peptidomimetics. Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg. pp. 1–32. doi:10.1007/7081_2015_176.
  14. ^ Mak, Jeffrey Y. W.; Pouwer, Rebecca H.; Williams, Craig M. (2014-12-08). "Natural Products with Anti-Bredt and Bridgehead Double Bonds". Angewandte Chemie International Edition. 53 (50): 13664–13688. doi:10.1002/anie.201400932. ISSN 1521-3773.
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