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" |