Unusual chemo- and stereoselectivity in the addition of chiral aminoalcohols to achiral nitroalkenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Preparation and structural determination of methyl 4,6-O-benzylidene-2,3-dideoxy-β-d-erythro-hexopyranosid[2,3-d]triazole and of its adducts with 3-nitrohex-2-enopyranosides
2. Nitroalkenes in the Synthesis of Heterocyclic Compounds
3. A new synthesis of 2,3-diamino-2,3-dideoxy-D-glucose
4. The Stereochemistry of Conjugate Additions. A Study of the Addition of Amines to (2-Nitropropenyl)-benzene
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1. Pd-Catalyzed Three-Component Reaction of Anilines, Ethyl Vinyl Ether, and Nitro-Paraffin: Assembly of β-Nitroamines;Organic Letters;2018-01-25
2. A short access to 3,5-disubstituted piperazinones based on the aza-Michael addition of α-amino esters to β-substituted nitroalkenes;Tetrahedron Letters;2016-10
3. Stereoselective aza-Michael addition of anilines to 1-nitro cyclohexene by intramolecular protonation;Tetrahedron Letters;2015-11
4. Synthesis of Trifluoromethyl-Containing Vicinal Diamines by Asymmetric Decarboxylative Mannich Addition Reactions;The Journal of Organic Chemistry;2015-03-04
5. Chiral cobalt(II)-salen-catalyzed Michael addition of amines to β-substituted nitroalkenes;Tetrahedron Letters;2014-04
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