Carbopalladation of Nitriles: Synthesis of 3,4-Disubstituted 2-Aminonaphthalenes and 1,3-Benzoxazine Derivatives by the Palladium-Catalyzed Annulation of Alkynes by (2-Iodophenyl)acetonitrile-Reference-Cited by-同舟云学术

Carbopalladation of Nitriles: Synthesis of 3,4-Disubstituted 2-Aminonaphthalenes and 1,3-Benzoxazine Derivatives by the Palladium-Catalyzed Annulation of Alkynes by (2-Iodophenyl)acetonitrile

Published:2002-12-13 Issue:2 Volume:68 Page:339-347
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tian Qingping¹,Pletnev Alexandre A.¹,Larock Richard C.¹

Affiliation:

1. Department of Chemistry, Iowa State University, Ames, Iowa 50011

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo026229%2B

Reference39 articles.

1. Synthesis of 2-Aminonaphthalene-1-thiol and Its Conversion into 8-Nitro-7H-benzo[c]phenothiazine

2. The Willgerodt-Kindler Reaction between Polycyclic Aromatic Amines and Benzaldehyde. Formation of 1,3-Thiazines

3. Quinazolines. IV. a novel synthesis of 1,3-diamino-benzo[f]quinazolines fromN1,N5-bis(2-naphthyl)biguanides

4. The Electrochemical Synthesis of Benzindoles from aminonaphthalenes in the presence of arsonium ylide

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