Enantioselective Organocatalyzed α Sulfenylation of Aldehydes
Danish National Research Foundation · Aarhus University · +1 more institution
Abstract
The facile elaboration of optically active α-sulfanyl-substituted aldehydes makes their direct preparation from unmodified aldehydes and 1-benzylsulfanyl-1,2,4-triazole particularly valuable. The substituted aldehydes are formed with excellent enantioselectivities in the presence of sterically demanding chiral pyrrolidine derivatives as organocatalysts (see scheme). R, R′=H, alkyl, allyl, benzyl, Ph. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2005/z462101_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing…
Citation impact
- FWCI
- 37.57
- Percentile
- 100%
- References
- 41
Authors
4- MMMauro MarigoCorresponding
Danish National Research Foundation, Aarhus University
- TCTobias C. Wabnitz
Danish National Research Foundation, National Research Foundation, Aarhus University
- DFDoris Fielenbach
Danish National Research Foundation, Aarhus University, National Research Foundation
- KAKarl Anker Jørgensen
National Research Foundation
Topics & keywords
- Enantioselective synthesis
- Pyrrolidine
- Steric effects
- Chemistry
- Sulfanyl
- Elaboration
- Organic chemistry
- Optically active