Enantioselective synthesis of the central ring system of lomaiviticin A in the form of an unusually stable cyclic hydrate
Angew Chem Int Ed Engl
.
2008;47(9):1680-4.
doi: 10.1002/anie.200704830.
Authors
Evan S Krygowski
1
,
Kerry Murphy-Benenato
,
Matthew D Shair
Affiliation
1
Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA.
PMID:
18214870
DOI:
10.1002/anie.200704830
No abstract available
Publication types
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
MeSH terms
Crystallography, X-Ray
Fluorenes / chemical synthesis*
Fluorenes / chemistry
Molecular Structure
Stereoisomerism
Substances
Fluorenes
lomaiviticin A
Grants and funding
CA125240/CA/NCI NIH HHS/United States