Domino Carbocationic Rearrangement of Aryl-2-(1-N-methyl/benzyl-3-indolyl)cyclopropyl Ketones: A Serendipitous Route to 1H-Cyclopenta[c]carbazole Framework-Reference-Cited by-同舟云学术

Domino Carbocationic Rearrangement of Aryl-2-(1-N-methyl/benzyl-3-indolyl)cyclopropyl Ketones: A Serendipitous Route to 1H-Cyclopenta[c]carbazole Framework

Published:2002-11-23 Issue:26 Volume:67 Page:9477-9480
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Venkatesh C.¹,Ila H.¹,Junjappa H.¹,Mathur Sanjay¹,Huch Volka¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kanpur-208016, India, and Institute of Inorganic Chemistry, Saarland University, D-66041 Saarbruecken, Germany hila@iitk.ac.in

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo025827l

Reference44 articles.

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2. Six-membered rings via olefin participation in the opening of acylcyclopropanes

3. Aryl participation in concerted cyclization of cyclopropyl ketones

4. Olefin participation in the acid-catalyzed opening of acylcyclopropanes. III. Formation of the bicyclo[2.2.1]heptane system

5. Olefin participation in the acid-catalyzed opening of acylcyclopropanes. IV. Cyclization of 5-methyl-6--(-3-pentenyl)bicyclo(3.1.0)hexan-2-one.

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