One-shot access to isoquinolone and (hetero)izidinone architectures using cyclic α-chloro eneformamides and cyclic anhydrides-Reference-Cited by-同舟云学术

One-shot access to isoquinolone and (hetero)izidinone architectures using cyclic α-chloro eneformamides and cyclic anhydrides

Published:2019 Issue:14 Volume:43 Page:5282-5286
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Beng Timothy K.¹²³⁴^ORCID,Langevin Spencer¹²³⁴,Farah Abdikani Omar¹²³⁴,Goodsell Joshua¹²³⁴^ORCID,Wyatt Katie¹²³⁴

Affiliation:

1. Department of Chemistry

2. Central Washington University

3. Ellensburg

4. USA

Abstract

A site-selective annulation reaction between cyclic α-chloro eneformamides and cyclic anhydrides which provides direct and modular access to pharmaceutically pertinent izidinones and isoquinolones, is presented.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ06539J

Reference37 articles.

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3. One-Pot Preparation of Quinolizidin-2-one and Indolizidin-7-one Ring Systems. Concise Total Syntheses of (.+-.)-Myrtine, (.+-.)-Lasubine II, and (-)-Indolizidine 223AB

4. Synthesis of Phenanthro[9,10-b]indolizidin-9-ones, Phenanthro[9,10-b]quinolizidin-9-one, and Related Benzolactams by Pd(OAc)2-Catalyzed Direct Aromatic Carbonylation

5. A highly stereocontrolled, four-step synthesis of (.+-.)-lasubine II

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