Control of Diastereoselectivity in Tandem Asymmetric Reactions Generating Nonadjacent Stereocenters with Bifunctional Catalysis by Cinchona Alkaloids
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- 1 January 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 129 (4), 768-769
- https://doi.org/10.1021/ja0670409
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Catalytic Asymmetric Staudinger Reactions to Form β-Lactams: An Unanticipated Dependence of Diastereoselectivity on the Choice of the Nitrogen SubstituentJournal of the American Chemical Society, 2005
- Catalytic Enantioselective C−C Bond Forming Conjugate Additions with Vinyl SulfonesJournal of the American Chemical Society, 2005
- Highly Enantioselective Conjugate Addition of Malonate and β-Ketoester to Nitroalkenes: Asymmetric C−C Bond Formation with New Bifunctional Organic Catalysts Based on Cinchona AlkaloidsJournal of the American Chemical Society, 2004
- Enantioselective Synthesis of 1,5-anti- and 1,5-syn-Diols Using a Highly Diastereoselective One-Pot Double Allylboration Reaction SequenceJournal of the American Chemical Society, 2002