241824-87-3Relevant articles and documents
Highly stereocontrolled access to a tetrahydroxy long chain base using anti-selective additions
Shimizu, Makoto,Kawamoto, Manabu,Niwa, Yasuki
, p. 1151 - 1152 (2007/10/03)
Complete diastereostereoselection was attained for the addition of acetylide and benzyloxymethyl anions to a chiral aldehyde and an imine derived from meso-tartaric acid, leading to a facile synthesis of (2S,3S,4R,5R,6Z)-2-amino-1,3,4,5-tetrahydroxyoctadecene as its pentaacetyl derivative in enantiomerically pure form.