Pd-catalyzed stereoselective tandem ring-opening amination/cyclization of vinyl γ-lactones: access to caprolactam diversity-Reference-Cited by-同舟云学术

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Pd-catalyzed stereoselective tandem ring-opening amination/cyclization of vinyl γ-lactones: access to caprolactam diversity

Published:2020 Issue:33 Volume:11 Page:8839-8845
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Xie Jianing¹²³⁴^ORCID,Li Xuetong¹²³⁴,Kleij Arjan W.¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Chemical Research of Catalonia (ICIQ)

2. The Barcelona Institute of Science and Technology

3. 43007–Tarragona

4. Spain

5. Catalan Institute of Research and Advanced Studies (ICREA)

Abstract

A Pd-mediated stereoselective tandem process has been developed towards a large variety of functional caprolactam synthons.

Funder

Ministerio de Economía y Competitividad

Generalitat de Catalunya

Institució Catalana de Recerca i Estudis Avançats

Agència de Gestió d'Ajuts Universitaris i de Recerca

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/SC/D0SC03647A

Reference68 articles.

2. Synthesis of Medium-Sized Ring Lactams

3. New drugs in migraine treatment and prophylaxis: telcagepant and topiramate

4. Design, Synthesis, and Biological Evaluation of Caprolactam-Modified Bengamide Analogues

5. 3,4-Dihydro-2(1H)-quinolinone as a Novel Antidepressant Drug: Synthesis and Pharmacology of 1-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-3,4- dihydro-5-methoxy-2(1H)-quinolinone and Its Derivatives

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