Sulfinamide
Sulfinamide is a functional group in organic chemistry containing a sulfur-oxygen double bond and a sulfur-nitrogen single bond. Sulfinamides are amides of sulfinic acid.
Chiral sulfinamides such as tert-butanesulfinamide, p-toluenesulfinamide[1][2] and 2,4,6-trimethylbenzenesulfinamide[3] are relevant to asymmetric synthesis.
References
- ^ Fanelli, D. L.; Szewczyk, J. M.; Zhang, Y.; Reddy, G. V.; Burns, D. M.; Davis, F. A. (2000). "SULFINIMINES (THIOOXIMINE S-OXIDES): ASYMMETRIC SYNTHESIS OF METHYL (R)-(+)-β-PHENYLALANATE FROM (S)-(+)-N-(BENZYLIDENE)-p-TOLUENESULFINAMIDE". Organic Syntheses. 77: 50
{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 10, p. 47. - ^ Ruano, J. L.; Alemán, J.; Parra, A.; Cid, M. B. (2007). "PREPARATION OF N-p-TOLYLSULFONYL-(E)-1-PHENYLETHYLIDENEIMINE". Organic Syntheses. 84: 129
{{cite journal}}: CS1 maint: multiple names: authors list (link). - ^ Ramachandar, T.; Wu, Y.; Zhang, J.; Davis, F. A. (2006). "(S)-(+)-2,4,6-TRIMETHYLBENZENESULFINAMIDE". Organic Syntheses. 83: 131
{{cite journal}}: CS1 maint: multiple names: authors list (link).
 | This organic chemistry article is a stub. You can help Wikipedia by expanding it. |