111462-27-2Relevant academic research and scientific papers
Stereoselective total synthesis of (+)-synargentolide A
Prasad, Kavirayani R.,Penchalaiah, Kamala
experimental part, p. 2853 - 2858 (2011/03/18)
The stereoselective synthesis of synargentolide A, a polyhydroxy δ-lactone, has been accomplished from tartaric acid. The key steps in the synthesis involve Keck and Brown allylations and ring closing metathesis.
New Chirons from D-Glucose. Regio- and Diastereoselective C-C Bond Forming Reactions Exploiting Novel Aldotetrafuranose Acetates as Chiral Synthetic Equivalents of Tartaric Aldehydes
Dhavale, Dilip D.,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille
, p. 4100 - 4105 (2007/10/02)
Two differentially protected tetrafuranose acetates 5 and 6 have been prepared from diacetone D-glucose in parallel short routes.They clearly act as chiral synthetic equivalents of D- and meso-tartaric aldehydes when exploited in Lewis acid promoted react
STEREOSELECTIVE ALLYLATION FOR PREPARATION OF L-HEXOSE DERIVATIVES
Williams, D. R.,Klinger, Franz D.
, p. 869 - 872 (2007/10/02)
The reaction of allyltrimethylsilane with α,β-dialkoxyaldehydes is catalyzed by magnesium bromide, and provides for a highly stereoselective allylation which is predicted by α-chelation of the Lewis acid.The observed stereocontrol is opposite to that gene
