Published in
American Chemical Society, Organic Letters, 13(12), p. 2944-2947, 2010
DOI: 10.1021/ol1009398
Links
- ORCID
- American Chemical Society
- [www.ncbi.nlm.nih.gov] | PDF
- [www.researchgate.net] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [europepmc.org] | PDF
Tools
Light-Induced Isomerization of Apoptolidin A leads to Inversion of C2-C3 Double Bond Geometry
Journal article published in 2010 by
Brian O. Bachmann 
,
Ruth McNees,
Bruce J. Melancon,
Victor P. Ghidu,
Rachel Clark,
Brenda C. Crews,
Sean M. DeGuire,
Lawrence J. Marnett,
Gary A. Sulikowski
,
Ruth McNees,
Bruce J. Melancon,
Victor P. Ghidu,
Rachel Clark,
Brenda C. Crews,
Sean M. DeGuire,
Lawrence J. Marnett,
Gary A. Sulikowski
This paper is available in a repository.
Full text: Download
Preprint: archiving allowed
- Must obtain written permission from Editor
- Must not violate ACS ethical Guidelines
Postprint:
archiving restricted
- Must obtain written permission from Editor
- Must not violate ACS ethical Guidelines
Published version:
archiving forbidden
Data provided by 
Abstract
The isolation, characterization, and cytotoxicity against H292 cells of apoptolidin G are reported. Apoptolidin G is shown to be derived by a light-induced isomerization of the C2-C3 carbon-carbon double bond of apoptolidin A.