Literature DB >> 27541576

Efficient synthesis of pyrrolo[1,2-a]quinoxalines catalyzed by a Brønsted acid through cleavage of C-C bonds.

Caixia Xie1, Lei Feng, Wanli Li, Xiaojun Ma, Xinkun Ma, Yihan Liu, Chen Ma.   

Abstract

An efficient and convenient one-pot domino reaction for the direct synthesis of pyrrolo[1,2-a]quinoxalines has been developed. This approach utilizes an imine formation reaction, SEAr reaction and cleavage of C-C bonds catalyzed by a Brønsted acid. β-Diketones and β-keto esters are both well tolerated to give the corresponding products in moderate to excellent yields.

Entities:  

Year:  2016        PMID: 27541576     DOI: 10.1039/c6ob01401a

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


  3 in total

1.  One-pot sequential coupling reactions as a new practical protocol for the synthesis of unsymmetrical 2,3-diethynyl quinoxalines and 4-ethynyl-substituted pyrrolo[1,2-a]quinoxalines.

Authors:  Ali Keivanloo; Saeed Lashkari; Mohammad Bakherad; Mahsa Fakharian; Sima Abbaspour
Journal:  Mol Divers       Date:  2020-04-16       Impact factor: 2.943

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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