Synthesis of Cu-catalysed quinazolinones using a Csp3–H functionalisation/cyclisation strategy-Reference-Cited by-同舟云学术

Synthesis of Cu-catalysed quinazolinones using a Csp3–H functionalisation/cyclisation strategy

Published:2017 Issue:34 Volume:15 Page:7140-7146
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Gholap Aniket V. A.¹²³⁴,Maity Soham¹⁵⁶⁴,Schulzke Carola⁷⁸⁹¹⁰^ORCID,Maiti Debabrata¹⁵⁶⁴^ORCID,Kapdi Anant R.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Institute of Chemical Technology

3. Mumbai-400019

4. India

5. Indian Institute of Technology Bombay

6. Mumbai 400076

7. Institute fur Biochemie

8. Ernst-Moritz-Arndt Universität Greifswald

9. D-17487 Greifswald

10. Germany

Abstract

A series of 2,3-disubstituted-4(3H)-quinazolinones were synthesised via a copper-catalysed C_sp3–H functionalisation/cyclisation of 2-amino-N,N-dialkylbenzamides.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01723E

Reference60 articles.

1. In silico design, synthesis, and biological evaluation of radioiodinated quinazolinone derivatives for alkaline phosphatase–mediated cancer diagnosis and therapy

2. The chemistry of recently isolated naturally occurring quinazolinone alkaloids

3. Recent developments in the chemistry of quinazolinone alkaloids

4. Structure–Activity Relationship for the 4(3H)-Quinazolinone Antibacterials

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