Improved dienophilicity of nitrocycloalkenes: Prospects for the development of a trans-Diels-Alder paradigm Journal Article


Authors: Kim, W. H.; Jun, H. L.; Danishefsky, S. J.
Article Title: Improved dienophilicity of nitrocycloalkenes: Prospects for the development of a trans-Diels-Alder paradigm
Abstract: (Chemical Equation Presented) The development of an efficient and stereoselective trans-Diels-Alder paradigm is described. A central element of this transformation is the introduction of a temporary dienophilic functionality (A), which serves both to activate the substrate for Diels-Alder cycloaddtion and, through its subsequent removal, to facilitate conversion of the cis-fused cycloadducts to the trans-fused series. © 2009 American Chemical Society.
Keywords: controlled study; substrate specificity; chemical reactions; chemical equations; diels alder reaction; nitrogen; stereochemistry; stereoisomerism; chemical modification; reaction time; cycloaddition; cycloadducts; diels-alder; stereo-selective; alkadiene; cycloalkene; extraction; cycloparaffins
Journal Title: Journal of the American Chemical Society
Volume: 131
Issue: 35
ISSN: 0002-7863
Publisher: American Chemical Society  
Date Published: 2009-09-09
Start Page: 12576
End Page: 12578
Language: English
DOI: 10.1021/ja9058926
PUBMED: 19685875
PROVIDER: scopus
PMCID: PMC2746560
DOI/URL:
Notes: --- - "Export Date: 30 November 2010" - "CODEN: JACSA" - "Source: Scopus"
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  1. Woo Han Kim
    8 Kim