P(RNCH2CH2)3N: An Efficient Promoter for the Nitroaldol (Henry) Reaction
Author:
Affiliation:
1. Department of Chemistry, Iowa State University, Ames, Iowa 50011
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9818733
Reference31 articles.
1. (a) Rosini, G. InComprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 2, pp 321−340.
2. Catalytic asymmetric nitroaldol reaction of α,α-difluoro aldehydes mediated by rare earth-lithium-BINOL complexes
3. A chiral nitronate dianion from (=d)-glyceraldehyde. Enantiospecific syntheses of 2,3-dideoxy-3-nitro furanosides and pyranosides
4. A New Stereoselective Synthesis of (E)-.alpha.,.beta.-Unsaturated-.gamma.-dicarbonyl Compounds by the Henry Reaction
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