Substrate-Controlled Domino Reaction of N-Sulfonyl Ketimines with 2-Aroyl-1-chlorocyclopropanecarboxylates: Access to Cyclopenta[c]chromenes and Benzo[f]cyclopenta[d][1,2]thiazepine Dioxides-Reference-Cited by-同舟云学术

Substrate-Controlled Domino Reaction of N-Sulfonyl Ketimines with 2-Aroyl-1-chlorocyclopropanecarboxylates: Access to Cyclopenta[c]chromenes and Benzo[f]cyclopenta[d][1,2]thiazepine Dioxides

Published:2021-04-12 Issue:9 Volume:86 Page:6721-6733
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Prakash Meher¹,Lodhi Rajni¹,Samanta Sampak¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Indore, Simrol, Indore, Madhya Pradesh 453552, India

Funder

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00459

Reference77 articles.

1. Recent Advances in the Chemistry of Pentafulvenes

2. An overview of the cycloaddition chemistry of fulvenes and emerging applications

3. Molecular Transformation to Pyrroles, Pentafulvenes, and Pyrrolopyridines by [2+2] Cycloaddition of Propargylamines with Tetracyanoethylene

4. Stereochemical and electronic features of the [3 + 2] cycloaddition of pentafulvenes with acylnitrones

5. Trapping the Lewis acid generated transient species from pentafulvene derived diazanorbornenes with ortho-functionalized aryl iodides and aliphatic alcohols

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