A Diels-Alder route to angularly functionalized bicyclic structures Journal Article


Authors: Kim, W. H.; Lee, J. H.; Aussedat, B.; Danishefsky, S. J.
Article Title: A Diels-Alder route to angularly functionalized bicyclic structures
Abstract: A Diels-Alder-based route to trans-fused angularly functionalized bicyclic structures has been developed. This transformation features the use of a tetrasubstituted dienophile in the cycloaddition step. © 2010 Elsevier Ltd.
Keywords: unclassified drug; substitution reaction; amine; chemical structure; x ray crystallography; diels alder reaction; synthesis; cycloaddition; 3,4 dimethyl 6 nitrobicyclo[4.3.0]dnon 3 en 1 carbonitrile; 3,4 dimethyl 6 nitrobicyclo[4.4.0]dec 3 en 1 carbonitrile; 9a nitro 1,2,3,4,4a,5,6,7,8,9,9a,10 dodecahydroanthracene 4a carbonitrile; allyl 7a cyano 5,6 dimethyl 2,3,3a,4,7,7a hexahydro 1h inden 3a ylcarbamate; allyl 8a cyano 6,7 dimethyl 1,2,3,4,4a,5,8,8a octahydronaphthalen 4a ylcarbamate; nitration; alnus
Journal Title: Tetrahedron
Volume: 66
Issue: 33
ISSN: 0040-4020
Publisher: Elsevier Inc.  
Date Published: 2010-08-14
Start Page: 6391
End Page: 6398
Language: English
DOI: 10.1016/j.tet.2010.04.094
PROVIDER: scopus
PMCID: PMC2921539
PUBMED: 20717474
DOI/URL:
Notes: --- - "Cited By (since 1996): 2" - "Export Date: 20 April 2011" - "CODEN: TETRA" - "Source: Scopus"
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  1. Woo Han Kim
    8 Kim