advances in metal-catalyzed cross-coupling reactions of halogenated quinazolinones and their quinazoline derivatives

advances in metal-catalyzed cross-coupling reactions of halogenated quinazolinones and their quinazoline derivatives

;Malose Jack Mphahlele;Marole Maria Maluleka
Journal of ethnopharmacology 2014 Vol. 19 pp. 17435-17463
163
mphahlele2014moleculesadvances

Abstract

Halogenated quinazolinones and quinazolines are versatile synthetic intermediates for the metal-catalyzed carbon–carbon bond formation reactions such as the Kumada, Stille, Negishi, Sonogashira, Suzuki-Miyaura and Heck cross-coupling reactions or carbon-heteroatom bond formation via the Buchwald-Hartwig cross-coupling to yield novel polysubstituted derivatives. This review presents an overview of the application of these methods on halogenated quinazolin-4-ones and their quinazolines to generate novel polysubstituted derivatives.

Citation

ID: 143459
Ref Key: mphahlele2014moleculesadvances
Use this key to autocite in SciMatic or Thesis Manager

References

Blockchain Verification

Account:
NFT Contract Address:
0x95644003c57E6F55A65596E3D9Eac6813e3566dA
Article ID:
143459
Unique Identifier:
10.3390/molecules191117435
Network:
Scimatic Chain (ID: 481)
Loading...
Blockchain Readiness Checklist
Authors
Abstract
Journal Name
Year
Title
5/5
Creates 1,000,000 NFT tokens for this article
Token Features:
  • ERC-1155 Standard NFT
  • 1 Million Supply per Article
  • Transferable via MetaMask
  • Permanent Blockchain Record
Blockchain QR Code
Scan with Saymatik Web3.0 Wallet

Saymatik Web3.0 Wallet