Literature DB >> 28805833

Application of α-amino acids for the transition-metal-free synthesis of pyrrolo[1,2-a]quinoxalines.

Huanhuan Liu1, Feiyu Zhou, Wen Luo, Yuxin Chen, Chenyang Zhang, Chen Ma.   

Abstract

A practical and concise protocol for the efficient synthesis of pyrrolo[1,2-a]quinoxalines from readily available α-amino acids and 2-(1H-pyrrol-1-yl)anilines under transition metal-free conditions has been established. This protocol, which includes the formation of new C-C and C-N bonds, features a wide substrate scope with a broad range of functional group tolerance.

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Year:  2017        PMID: 28805833     DOI: 10.1039/c7ob01688c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  α-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and other N-heterocycles via decarboxylative oxidative annulation reaction.

Authors:  Mayavan Viji; Manjunatha Vishwanath; Jaeuk Sim; Yunjeong Park; Chanhyun Jung; Seohu Lee; Heesoon Lee; Kiho Lee; Jae-Kyung Jung
Journal:  RSC Adv       Date:  2020-10-07       Impact factor: 4.036

Review 2.  Recent advances in the transition-metal-free synthesis of quinoxalines.

Authors:  Biplob Borah; L Raju Chowhan
Journal:  RSC Adv       Date:  2021-11-19       Impact factor: 4.036

3.  Tin(ii) chloride dihydrate/choline chloride deep eutectic solvent: redox properties in the fast synthesis of N-arylacetamides and indolo(pyrrolo)[1,2-a]quinoxalines.

Authors:  Sergio Alfonso Trujillo; Diana Peña-Solórzano; Oscar Rodríguez Bejarano; Cristian Ochoa-Puentes
Journal:  RSC Adv       Date:  2020-11-06       Impact factor: 3.361

  3 in total

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