Asymmetric Michael reaction of α-cyano carboxylates catalyzed by a rhodium complex with trans-chelating chiral diphosphine PhTRAP
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference64 articles.
1. The asymmetric Michael addition reactions using chiral imines
2. Asymmetrische Michael‐Additionen. Stereoselektive Alkylierungen des ( R )‐ und ( S )‐Enamins aus Cyclohexanon und 2‐(Methoxymethyl)pyrrolidin durch α‐(Methoxycarbonyl)zimtsäure‐methylester
3. Asymmetric synthesis of β-substituted δ-ketoesters via michael-additions of samp/ramp-hydrazones to α,β-unsaturated esters, virtually complete 1.6-asymmetric induction
4. Asymmetric Michael additions via SAMP-/RAMP-hydrazones anti-diastereo- and enantioselective synthesis of 3,4-disubstituted 5-oxo-alkanoates
5. Enantioselective synthesis of quaternary carbon centers through Michael-type alkylation of chiral imines
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2. Control of chemoselectivity in asymmetric tandem reactions: Direct synthesis of chiral amines bearing nonadjacent stereocenters;Proceedings of the National Academy of Sciences;2018-02-05
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