697298-69-4Relevant academic research and scientific papers
Highly stereoselective intermolecular oxy-michael addition reaction to α,β-unsaturated malonate esters
Buchanan, David J.,Dixon, Darren J.,Hernandez-Juan, Felix A.
, p. 1357 - 1360 (2004)
The highly diastereoselective oxy-Michael addition of the "naked" anion of (6S)-methyl δ lactol to alkylidiene-, arylidene-, and heteroarylidene-malonate derivatives leading to the direct formation of THP*-protected β-hydroxy ester derivatives is describe
PRODUCTION OF OXY-MICHAEL ADDUCTS
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Page 22-24, (2010/02/08)
The invention provides a method of producing an oxy-Michael adduct comprising allowing a Michael acceptor to react with an alkoxide of an alcohol of formula R0H having a chiral centre at the hydroxy carbon, in the presence of a multidentate ligand. The
