Stereospecific synthesis of (+)-oxybiotin from D-xylose. Preparation of the final chiral (+)-oxybiotin precursor
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. The Microbiological Activity of an Oxygen Analog of Biotin
2. FURAN AND TETRAHYDROFURAN DERIVATIVES. IV. THE SYNTHESIS OF HEXAHYDRO-2-OXO-1-FURO[3,4]IMIDAZOLE DERIVATIVES
3. Furan and Tetrahydrofuran Derivatives. V. The Synthesis of a Racemic Hexahydro-2-oxo-4-methyl-1-furo [3,4] imidazole1,2
4. Furan and Tetrahydrofuran Derivatives. VI. The Total Synthesis of dl-Oxybiotin1
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1. A short enantioselective synthesis of 3-epi-jaspine B and (+)-oxybiotin via an intramolecular tandem desilylation oxa-Michael addition strategy;RSC Adv.;2014
2. A versatile route for the stereoselective synthesis of oxybiotin;Tetrahedron: Asymmetry;2008-06
3. A total synthesis of (+)-oxybiotin from d-arabinose;Tetrahedron;2004-06
4. An efficient synthesis of (+)-oxybiotin from d-arabinose;Tetrahedron Letters;2002-03
5. Stereospecific synthesis of (+)-oxybiotin from d-xylose;Carbohydrate Research;2002-03
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