804551-13-1Relevant articles and documents
Highly stereoselective oxy-Michael additions to α,β- disubstituted nitro olefins: Asymmetric synthesis of pseudo-norephedrine derivatives and THP protected α-hydroxy ketones
Buchanan, David J.,Dixon, Darren J.,Hernandez-Juan, Felix A.
, p. 2932 - 2934 (2004)
The "naked" anion of (S)-6-methyl delta lactol undergoes efficient oxy-Michael addition to α,β-disubstituted nitro olefins to give the THP* protected Henry products with excellent (95→98% de) stereocontrol at the β-position and moderate (up to 3:1) stereo