Is an Iodine Atom Almighty as a Leaving Group for Bu3SnH-Mediated Radical Cyclization? The Effect of a Halogen Atom on the 5-Endo-trig Radical Cyclization of N-Vinyl-α-halo Amides-Reference-Cited by-同舟云学术

Is an Iodine Atom Almighty as a Leaving Group for Bu3SnH-Mediated Radical Cyclization? The Effect of a Halogen Atom on the 5-Endo-trig Radical Cyclization of N-Vinyl-α-halo Amides

Published:2002-07-09 Issue:16 Volume:67 Page:5537-5545
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tamura Osamu¹,Matsukida Hana¹,Toyao Atsushi¹,Takeda Yoshifumi¹,Ishibashi Hiroyuki¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Kanazawa University, Takara-machi, Kanazawa 920-0934, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo020007u

Reference24 articles.

1. Radical cyclizations of N-vinylic α-chloroacetamides. 5-endo-trig and 4-exo-trig cyclizations

2. β-Lactams by a nickel powder/acetic acid mediated radical cyclisation

3. Copper(I) reactions in N-heterocycle synthesis: efficient preparation of substituted pyrrolidinones

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