Harnessing Glycal-Epoxide Rearrangements: The Generation of the AB, EF, and IJ Rings of Adriatoxin
Die Leiter hoch: Der Aufbau dreier bicyclischer Untereinheiten von Adriatoxin gelang mithilfe von Glycal‐Epoxid‐ und Glycal‐Claisen‐Umlagerungen sowie C‐Glycosid bildenden Reaktionen.
Saved in:
Published in: | Angewandte Chemie Vol. 120; no. 42; pp. 8175 - 8178 |
---|---|
Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
06-10-2008
WILEY‐VCH Verlag |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Die Leiter hoch: Der Aufbau dreier bicyclischer Untereinheiten von Adriatoxin gelang mithilfe von Glycal‐Epoxid‐ und Glycal‐Claisen‐Umlagerungen sowie C‐Glycosid bildenden Reaktionen. |
---|---|
Bibliography: | We are grateful to the National Institutes of Health, General Medical Sciences (GM56677) for support of this work. C.O.A. acknowledges Pfizer for a graduate fellowship. We would like to thank the support staff at the University of Utah and especially Dr. Charles Mayne (NMR) and Dr. Jim Muller (MS) for their help in obtaining data. ark:/67375/WNG-N1B25682-C National Institutes of Health, General Medical Sciences - No. GM56677 ArticleID:ANGE200803791 istex:830066F4C425B1F71F392635E651E752EFB8BE44 |
ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.200803791 |