Regioselective Unusual Formation of Spirocyclic 4-{2‘-Benzo(2‘,3‘-dihydro)furo}- 9-methyl-2,3,9-trihydrothiopyrano[2,3-b]indole by 4-exo-trig Aryl Radical Cyclization and Rearrangement-Reference-Cited by-同舟云学术

Regioselective Unusual Formation of Spirocyclic 4-{2‘-Benzo(2‘,3‘-dihydro)furo}- 9-methyl-2,3,9-trihydrothiopyrano[2,3-b]indole by 4-exo-trig Aryl Radical Cyclization and Rearrangement

Published:2006-08-01 Issue:18 Volume:8 Page:4059-4062
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Majumdar K. C.¹,Alam S.¹

Affiliation:

1. Department of Chemistry, University of Kalyani, Kalyani 741235, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol061531g

Reference43 articles.

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2. Formal Total Synthesis of (±)-Vindoline by Tandem Radical Cyclization

3. Radical Cyclization Approach to Spirocyclohexadienones

4. Regiochemistry in aryl radical cyclisations (5-exo versus 6-endo) of N-vinylic 2-iodobenzamides

5. Aryl radical cyclisation onto pyrroles: a divergent synthesis of spiropyrrolidinyloxindoles and pyrroloquinolines

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