Construction of the 1,5-Benzodiazepine Skeleton from o-Phenylendiamine and Propargylic Alcohols via a Domino Gold-Catalyzed Hydroamination/Cyclization Process-Reference-Cited by-同舟云学术

Construction of the 1,5-Benzodiazepine Skeleton from o-Phenylendiamine and Propargylic Alcohols via a Domino Gold-Catalyzed Hydroamination/Cyclization Process

Published:2016-07-28 Issue:15 Volume:18 Page:3511-3513
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Cacchi Sandro¹,Fabrizi Giancarlo¹,Goggiamani Antonella¹,Iazzetti Antonia¹

Affiliation:

1. Dipartimento di Chimica e Tecnologie del Farmaco, La Sapienza, Università di Roma, P.le A. Moro 5, 00185 Rome, Italy

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Sapienza Università di Roma

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01720

Reference23 articles.

1. Synthesis of spiro[indolo-1,5-benzodiazepines] from 3-acetyl coumarins for use as possible antianxiety agents

2. Synthesis and antimicrobial, antifungal and anthelmintic activities of 3h-1,5-benzodiazepine derivatives

3. Studies of antimicrobial activities of some 4-thiazolidinone fused pyrimidines, [1,5]-benzodiazepines and their oxygen substituted hydroxylamine derivatives

4. On the synthetic way to novel peri-annelated imidazo[1,5]benzo-diazepinones as the potent non-nucleoside reverse transcriptase inhibitors

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