N,N-DIALKYLTHIOAMIDES IN THE MICHAEL ADDITION TO CONJUGATE CARBONYL COMPOUNDS, REGIOSELECTIVITY, STEREOCHEMISTRY AND MECHANISM
Author:
Affiliation:
1. a Institute of Organic Chemistry with Centre of Phytochemistry , Bulgarian Academy of Sciences, Sofia, 1113, Bulgaria
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426509308032434
Reference19 articles.
1. Oare , D. A. and Heathcock , C. H. 1989. Topics in Stereochemistry, Edited by: Eliel , E. L. and Wilen , S. H. Vol. 19, 227New York: Wiley.
2. Regio- and stereoselectivity in the addition of metal n,n-dimethylphenylacetamide enolates to some conjugated carbonyl compounds
3. Triple ion chelate structure of an equilibrium Michael adduct
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1. ChemInform Abstract: N,N-Dialkylthioamides in the Michael Addition to Conjugate Carbonyl Compounds: Regioselectivity, Stereochemistry and Mechanism.;ChemInform;2010-08-20
2. Michael Addition of Selenoamides to α,β-Unsaturated Carbonyl Compounds: Stereocontrolled Synthesis of δ-Oxo Selenoamides and Their Reactivity;Organic Letters;2000-01-06
3. Kinetic asymmetric protonation as a stereochemistry determining step in theMichael addition of acetic acid derivatives to ?-substituted cinnamic acid derivatives;Monatshefte f�r Chemie Chemical Monthly;1995
4. Titanium enolates and “ate” complexes of N,N-disubstituted amides and thioamides in the Michael reaction.;Tetrahedron;1994-01
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