A group of modified (salen)Cr(III)Cl complexes with bulky benzylic substituents in the 3,3'-position of the salicylidene moiety have been successfully applied for the asymmetric nitroaldol reaction. The readily accessible complex bearing 3-phenylpent-3-yl groups (2 mol %) leads to beta-nitro alcohols in up to 92% yield and 94% ee.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/jo802107b | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!