Document Detail


Preparation of the 5/5-spiroketal of the ritterazines.
MedLine Citation:
PMID:  17397225     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The enantiomerically pure 5/5-spiroketal required for the synthesis of the ritterazines has been prepared with high diastereocontrol by ring closure followed by equilibration.
Authors:
Douglass F Taber; Jean-Michel Joerger
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2007-03-31
Journal Detail:
Title:  The Journal of organic chemistry     Volume:  72     ISSN:  0022-3263     ISO Abbreviation:  J. Org. Chem.     Publication Date:  2007 Apr 
Date Detail:
Created Date:  2007-04-20     Completed Date:  2007-06-29     Revised Date:  2013-06-06    
Medline Journal Info:
Nlm Unique ID:  2985193R     Medline TA:  J Org Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  3454-7     Citation Subset:  IM    
Affiliation:
Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, USA. taberdf@udel.edu
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MeSH Terms
Descriptor/Qualifier:
Chemistry, Organic / methods*
Crystallography, X-Ray
Furans / chemical synthesis*
Magnetic Resonance Spectroscopy
Molecular Structure
Spiro Compounds / chemical synthesis*,  chemistry
Grant Support
ID/Acronym/Agency:
GM 60287/GM/NIGMS NIH HHS; R01 GM060287-01/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Furans; 0/Spiro Compounds; 0/spiroketal
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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