Microwave-assisted one-pot two-step imine formation–hetero-Diels–Alder–detosylation/aromatization sequence: direct access to dibenzo[<i>b</i>,<i>h</i>][1,6]naphthyridines-Reference-Cited by-同舟云学术

Microwave-assisted one-pot two-step imine formation–hetero-Diels–Alder–detosylation/aromatization sequence: direct access to dibenzo[b,h][1,6]naphthyridines

Published:2022 Issue:37 Volume:20 Page:7472-7482
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jan Gowsia¹,Kumar Atul¹^ORCID,Karuppasamy Muthu¹,Rajput Diksha¹,Slathia Nancy²,Kapoor Kamal K.²,Sridharan Vellaisamy¹^ORCID

Affiliation:

1. Department of Chemistry and Chemical Sciences, Central University of Jammu, Rahya-Suchani (Bagla), District-Samba, Jammu-181143, J&K, India

2. Department of Chemistry, University of Jammu, Jammu-180006, J&K, India

Abstract

A microwave-assisted, copper-catalyzed, one-pot, two-step synthesis of benzofused[1,6]naphthyridines is established.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01216B

Reference35 articles.

1. Cytotoxic Aaptamine Derivatives from the South China Sea Sponge Aaptos aaptos

2. Aaptamine Derivatives from the Indonesian Sponge Aaptos suberitoides

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4. Antiviral and Anticancer Optimization Studies of the DNA-binding Marine Natural Product Aaptamine

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