High Diastereoselectivity Induced by a Fluorous Alkyl Group in the Asymmetric Michael Reaction of Nitroalkenes Catalyzed by a Prolinol Methyl Ether
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajoc.201300171/fullpdf
Reference69 articles.
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1. Fluorous Catalysis;Green Techniques for Organic Synthesis and Medicinal Chemistry;2018-02-02
2. Recent Advances in Asymmetric Organocatalyzed Conjugate Additions to Nitroalkenes;Molecules;2017-05-29
3. Asymmetric Conjugate Additions of Carbonyl Compounds to Nitroalkenes under Solvent-Free Conditions Using Fluorous Diaminomethylenemalononitrile Organocatalyst;Chemical and Pharmaceutical Bulletin;2017
4. The Catalytic, Enantioselective Michael Reaction;Organic Reactions;2016-09-13
5. Enhancement of stereoselectivities in asymmetric synthesis using fluorinated solvents, auxiliaries, and catalysts;RSC Advances;2015
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