One-Pot Synthesis of Pyrrolo[1,2-a]quinoxaline Derivatives via Iron-Promoted Aryl Nitro Reduction and Aerobic Oxidation of Alcohols-Reference-Cited by-同舟云学术

One-Pot Synthesis of Pyrrolo[1,2-a]quinoxaline Derivatives via Iron-Promoted Aryl Nitro Reduction and Aerobic Oxidation of Alcohols

Published:2012-09-12 Issue:18 Volume:14 Page:4754-4757
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pereira Maria de Fatima¹,Thiéry Valérie¹

Affiliation:

1. Université de La Rochelle, UMR CNRS 7266 -LIENSs, LIttoral ENvironnement SociétéS, Pôle Sciences et Technologie, Bâtiment Marie-Curie, Avenue Michel Crépeau, 17042 La Rochelle, France, and Université de Caen Basse-Normandie, EA 4258 CERMN - FR CNRS 3038 INC3M, UFR des Sciences Pharmaceutiques, 14032 Caen, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol302006b

Reference30 articles.

1. Novel and Selective Partial Agonists of 5-HT3 Receptors. 2. Synthesis and Biological Evaluation of Piperazinopyridopyrrolopyrazines, Piperazinopyrroloquinoxalines, and Piperazinopyridopyrroloquinoxalines

2. Novel, Potent, and Selective Quinoxaline-Based 5-HT3 Receptor Ligands. 1. Further Structure−Activity Relationships and Pharmacological Characterization

3. Specific Targeting of Peripheral Serotonin 5-HT3 Receptors. Synthesis, Biological Investigation, and Structure−Activity Relationships

4. Quinoxaline chemistry. Part 16. 4-Substituted anilino and 4-substituted phenoxymethyl pyrrolo[1,2-a]quinoxalines and N-[4-(pyrrolo[1,2-a]quinoxalin-4-yl)amino and hydroxymethyl]benzoyl glutamates. Synthesis and evaluation of in vitro biological activity

5. Synthesis, Antimalarial Activity, and Molecular Modeling of New Pyrrolo[1,2-a]quinoxalines, Bispyrrolo[1,2-a]quinoxalines, Bispyrido[3,2-e]pyrrolo[1,2-a]pyrazines, and Bispyrrolo[1,2-a]thieno[3,2-e]pyrazines

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