A new and concise synthetic route to an enantiopure (+)-conduritol-E derivative from diethyl L-tartrate

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(+)-(1R,2R,3S,6S)-3,6-Di-O-methyl conduritol-E was efficiently synthesized in enantiomerically pure form starting from diethyl L-tartrate in 33% total yield using a ring-closing olefin metathesis reaction as one of the key steps. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
1999-12
Language
English
Article Type
Article
Keywords

RING-CLOSING METATHESIS; OLEFIN METATHESIS; ORGANIC-SYNTHESIS; INHIBITORS; ALCOHOLS; ACID

Citation

TETRAHEDRON-ASYMMETRY, v.10, no.23, pp.4473 - 4475

ISSN
0957-4166
DOI
10.1016/S0957-4166(99)00517-0
URI
http://hdl.handle.net/10203/68775
Appears in Collection
CH-Journal Papers(저널논문)
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