Asymmetric synthesis of 2-substituted cycloalkanecarboxaldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
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2. Asymmetric syntheses using tert-leucine. 1. An asymmetric synthesis of .beta.-substituted aldehydes via 1,4-addition of Grignard reagents to chiral .alpha.,.beta.-unsaturated aldimines
3. Asymmetric michael reaction via chiral α,β-unsaturated aldimines
4. Asymmetric synthesis of α-alkylated cyclic ketones via chiral chelated lithioenamines
5. Stereoselective reactions. I. A highly efficient asymmetric synthesis of .BETA.-substituted aldehydes via 1,4-addition of Grignard reagents to optically active .ALPHA.,.BETA.-unsaturated aldimines.
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1. Conjugate Addition II;Key Chiral Auxiliary Applications;2014
2. Leucine t-butyl ester;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
3. Regio- and diastereoselective SN2′ or SN2″ reactions on chiral acetals of cyclic aldehydes promoted by PhCu, BF3;Tetrahedron: Asymmetry;2001-08
4. tert-Leucinetert-Butyl Ester;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
5. An enantiospecific cobaloxime π-cation initiated carbocyclisation;Tetrahedron Letters;1998-04
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