Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation-Reference-Cited by-同舟云学术

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Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation

Published:2006-09 Issue:19 Volume:8 Page:4307-4310
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Johnson Jeffrey B.,Yu Robert T.,Fink Paul,Bercot Eric A.,Rovis Tomislav

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0616337

Reference38 articles.

1. ALKYLATION, ARYLATION, AND VINYLATION OF ACYL CHLORIDES BY MEANS OF ORGANOTIN COMPOUNDS IN THE PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(O)

2. A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium

3. Mild, selective, general method of ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium

4. A novel ketone synthesis by a palladium-catalyzed reaction of thiol esters and organozinc reagents

5. Thiol Ester−Boronic Acid Coupling. A Mechanistically Unprecedented and General Ketone Synthesis

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