Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Total synthesis of the C-37-C-45 F-ring fragment of spongistatins
 
research article

Total synthesis of the C-37-C-45 F-ring fragment of spongistatins

Lemaire-Audoire, S
•
Vogel, P  
1998
Tetrahedron Letters

The highly substituted F ring of Spongistatins was synthesized from (R)-(+)-3-benzyloxy-2-methylpropan-1-ol (5), using two sequential Sharpless dihydroxylations as key-steps. A 4-deoxy-4-methyl-D-threo-L-glucoheptopyranose derivative was obtained and could be used to generate the corresponding allyl beta-C-glycoside. (C) 1998 Elsevier Science Ltd. All rights reserved.

  • Details
  • Metrics
Type
research article
DOI
10.1016/S0040-4039(97)10817-6
Author(s)
Lemaire-Audoire, S
Vogel, P  
Date Issued

1998

Publisher

Elsevier

Published in
Tetrahedron Letters
Volume

39

Issue

11

Start page

1345

End page

1348

Subjects

altohyrtin-a

•

asymmetric dihydroxylation

•

inhibitors

•

tubulin

•

derivatives

•

binding

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219445
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés