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  Total Synthesis of Woodrosin I

Fürstner, A., Jeanjean, F., & Razon, P. (2002). Total Synthesis of Woodrosin I. Angewandte Chemie International Edition, 41(12), 2097-2101. doi:10.1002/1521-3773(20020617)41:12<2097:AID-ANIE2097>3.0.CO;2-T.

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 Creators:
Fürstner, Alois1, Author              
Jeanjean, Fabien1, Author              
Razon, Patrick1, Author              
Affiliations:
1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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Free keywords: glycosides; macrocycles; metathesis; natural products; ruthenium
 Abstract: The reliability of ring-closing metathesis, even in complex cases, is highlighted in the first total synthesis of the structurally intriguing resin glycoside woodrosin I (1). The synthesis also shows the maturity of the trichloroacetimidate method for glycosylation and features the most advanced application of an orthoester rearrangement for the formation of a β-glycosidic bond.

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Language(s): eng - English
 Dates: 2002-02-082002-06-122002-06-17
 Publication Status: Published in print
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: Angewandte Chemie International Edition
  Abbreviation : Angew. Chem. Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH Verlag
Pages: - Volume / Issue: 41 (12) Sequence Number: - Start / End Page: 2097 - 2101 Identifier: ISSN: 1521-3773
CoNE: https://pure.mpg.de/cone/journals/resource/0570-0833