Document Detail

Lewis acid catalyzed cycloaddition of methylenecyclopropanes with salicylaldehydes.
MedLine Citation:
PMID:  20462238     Owner:  NLM     Status:  MEDLINE    
Lewis acid catalyzed cycloaddition of methylenecyclopropanes (MCPs) with o-quinonemethide analogues, derived from the corresponding salicylaldehydes and CH(OEt)(3), produces the corresponding cycloadducts 3 in moderate to high yields at room temperature (20 degrees C). Moreover, the compounds 3 can be transformed to the indene derivatives 5 at high temperature. Plausible mechanisms have been proposed on the basis of control experiments.
Min Jiang; Min Shi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Organic letters     Volume:  12     ISSN:  1523-7052     ISO Abbreviation:  Org. Lett.     Publication Date:  2010 Jun 
Date Detail:
Created Date:  2010-05-28     Completed Date:  2010-08-17     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2606-9     Citation Subset:  IM    
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China.
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MeSH Terms
Aldehydes / chemistry*
Combinatorial Chemistry Techniques
Cyclopropanes / chemistry*
Gold / chemistry*
Molecular Structure
Reg. No./Substance:
0/Aldehydes; 0/Cyclopropanes; 0/methylenecyclopropane; 7440-57-5/Gold; 90-02-8/salicylaldehyde

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