Triple ion chelate structure of an equilibrium Michael adduct
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference25 articles.
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1. 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
2. N,N-DIALKYLTHIOAMIDES IN THE MICHAEL ADDITION TO CONJUGATE CARBONYL COMPOUNDS, REGIOSELECTIVITY, STEREOCHEMISTRY AND MECHANISM;Phosphorus, Sulfur, and Silicon and the Related Elements;1993-05-01
3. Structure of lithium hexamethyldisilazide in the presence of hexamethylphosphoramide. Spectroscopic and computational studies of monomers, dimers, and triple ions;Journal of the American Chemical Society;1993-05
4. Diastereoselective Three-Center Michael Addition ofβ-Ketoesters to Prostereogenicα,β-Unsaturated Carbonyl Compounds Catalyzed by K2CO3 or Cs2CO3;Angewandte Chemie International Edition in English;1992-12
5. K2CO3- oder Cs2CO3-katalysierte diastereoselektive Drei-Zentren-Michael-Addition von β-Ketoestern an prostereogene α,β ungesättigte Carbonylverbindungen;Angewandte Chemie;1992-12
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