Studies towards the synthesis of the highly oxygenated bicyclic core of zaragozic acid1: Incorporation of three quaternary chiral carbon centres
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Gurjar, M.K.; Das, S.K. and Sadalpure, K.S. Preceding Communication.
2. Zaragozic acid A, a potent inhibitor of squalene synthase: initial chemistry and absolute stereochemistry
3. The zaragozic acids: Structure elucidation of a new class of squalene synthase inhibitors
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1. Total Syntheses of Zaragozic Acids A and C by a Carbonyl Ylide Cycloaddition Strategy;Chemistry - A European Journal;2006-12-04
2. Total synthesis of zaragozic acid C by an aldol-based strategy;Tetrahedron;2005-11
3. Sugars as Chiral Starting Materials in Enantiospecific Synthesis;The Organic Chemistry of Sugars;2005-09-21
4. Recent Progress in the Synthesis of Zaragozic Acids and Analogs;Current Organic Chemistry;2001-06-01
5. An approach to the bicyclic core of the zaragozic acids via the aldol reaction between methyl (α-D-xylofuranoside)uronate and D-(R)-glyceraldehyde acetonide;Tetrahedron;1999-10
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