Studies on the intramolecular cycloaddition reaction of isomünchnones derived from N-alkenyl substituted diazoimides
A Padwa, DJ Austin, AT Price, MD Weingarten
Index: Padwa; Austin; Price; Weingarten Tetrahedron, 1996 , vol. 52, # 9 p. 3247 - 3260
Full Text: HTML
Citation Number: 29
Abstract
A series of N-alkenyl substituted diazoimides were prepared and subjected to Rh (II) catalyzed decomposition. The initially generated rhodium carbenoid undergoes ready cyclization onto the neighboring amide carbonyl oxygen atom to generate an isomünchnone intermediate. Subsequent 1, 3-dipolar cycloaddition across the pendant olefin affords the cycloadduct in high yield. The stereochemical assignment of several of the cycloadducts ...
Related Articles:
[Bunce, Richard A.; Smith, Christopher L.; Lewis, Jason R. Journal of Heterocyclic Chemistry, 2004 , vol. 41, # 6 p. 963 - 970]
Generalization of the Benzotriazole-Mediated Introduction of N-Substituents into Amides
[Katritzky, Alan R.; Ignatchenko, Alexey V.; Lang, Hengyuan Journal of Organic Chemistry, 1995 , vol. 60, # 13 p. 4002 - 4005]
[Hoffman, Robert V.; Nayyar, Naresh K. Journal of Organic Chemistry, 1994 , vol. 59, # 13 p. 3530 - 3539]
[Hoffman, Robert V.; Nayyar, Naresh K. Journal of Organic Chemistry, 1994 , vol. 59, # 13 p. 3530 - 3539]
The oxidative dealkylation of tertiary amides: mechanistic aspects
[Iley, Jim; Tolando, Roberto Journal of the Chemical Society. Perkin Transactions 2, 2000 , # 11 p. 2328 - 2336]