Synthesis of a ‘reverse ester’ analogue of 1,2-sn-diglycerides from (S)-1,2-di-O-isoprophylideneglycerol; efficient, stereospecific nucleophilic displacement via a triflate at glycerol C-2
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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2. The Krapcho Dealkoxycarbonylation Reaction of Esters with α-Electron-Withdrawing Substituents;Organic Reactions;2013-05-30
3. ChemInform Abstract: Synthesis of a ′Reverse Ester′ Analogue of 1,2-syn-Diglycerides from ( S)-1,2-Di-O-Isopropylideneglycerol; Efficient, Stereospecific Nucleophilic Displacement via a Triflate at Glycerol C-2.;ChemInform;2010-08-19
4. O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks;Org. Biomol. Chem.;2010
5. Recent synthetic applications of the dealkoxycarbonylation reaction. Part 1. Dealkoxycarbonylations of malonate esters;Arkivoc;2007-04-12
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