Mechanistic Studies on the O-Directed Free-Radical Hydrostannation of Disubstituted Acetylenes with Ph3SnH and Et3B and on the Iodination of Allylically Oxygenated α-Triphenylstannylalkenes-Reference-Cited by-同舟云学术

Mechanistic Studies on the O-Directed Free-Radical Hydrostannation of Disubstituted Acetylenes with Ph3SnH and Et3B and on the Iodination of Allylically Oxygenated α-Triphenylstannylalkenes

Published:2005-10-26 Issue:24 Volume:7 Page:5377-5380
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dimopoulos Paschalis¹,George Jonathan¹,Tocher Derek A.¹,Manaviazar Soraya¹,Hale Karl J.¹

Affiliation:

1. The Christopher Ingold Laboratories, The Chemistry Department, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol051937d

Reference14 articles.

1. O-Directed Free-Radical Hydrostannations of Propargyl Ethers, Acetals, and Alcohols with Ph3SnH and Et3B

2. A Study of Vinyl Radical Cyclization Using N-Alkenyl-7-bromo-Substituted Hexahydroindolinones

3. Nickel-Catalyzed Preparation of Bicyclic Heterocycles: Total Synthesis of (+)-Allopumiliotoxin 267A, (+)-Allopumiliotoxin 339A, and (+)-Allopumiliotoxin 339B

4. Total Syntheses of Pumiliotoxin A and Allopumiliotoxin Alkaloids. Interplay of Pharmacologically Active Natural Products and New Synthetic Methods and Strategies

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