The Michael addition-elimination of ylide to alpha,beta-unsaturated imines leads to a highly diastereoselective and enantioselective synthesis of vinylcyclopropanecarbaldehydes in good to high yields for the first time. A sequential cyclopropanation-aziridination protocol for the preparation of cyclopropylaziridines is also developed with good diastereoselectivity in good to high yields.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ja052228yDOI Listing

Publication Analysis

Top Keywords

michael addition-elimination
8
alphabeta-unsaturated imines
8
synthesis vinylcyclopropanecarbaldehydes
8
good high
8
high yields
8
addition-elimination ylides
4
ylides alphabeta-unsaturated
4
imines highly
4
highly stereoselective
4
stereoselective synthesis
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!