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Synlett 2003(2): 0215-0218
DOI: 10.1055/s-2003-36801
DOI: 10.1055/s-2003-36801
LETTER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of syn- and anti-3,5-Dihydroxy-6-heptenoates from 2-Deoxy-d-ribose: Intermediates for Polyols Synthesis
Further Information
Received
10 December 2002
Publication Date:
22 January 2003 (online)
Publication History
Publication Date:
22 January 2003 (online)
Abstract
Syntheses of all four diastereomers of syn- and anti-3,5-dihydroxy-6-heptenoate, proven versatile synthetic intermediates that are enantiomerically pure and functionally differentiated at both ends, have been developed.
Key words
1,3-diols synthesis - tetrahydro-2-furanylacetate - polyols - ring opening - 4-hydroxy-6-vinyltetrahydro-2H-2-pyranone
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