Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2006(3): 0246-0246
DOI: 10.1055/s-2006-931955
DOI: 10.1055/s-2006-931955
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Asymmetric Aza-Mannich Reactions of Sulfinimines
J. C. Lanter*, H. Chen, X. Zhang, Z. Sui
Johnson & Johnson Pharmaceutical Research and Development, RAritan, USA
Further Information
Publication History
Publication Date:
21 February 2006 (online)
Significance
Addition of enantiomerically pure sulfinimine anions to N-sulfonyl aldimines gave the addition product with excellent diastereoselectivity. The E-sulfonylimine is much more reactive than the Z-sulfonylimine, possibly due to the increased steric hinderance in the transition state of the Z-sulfonylimine. The single diastereoisomer obtained can be rationalized by the steric bulk and orientation of the tert-butylsulfonyl group.