Literature DB >> 24782111

A reagent-free oxidative cyclization approach to indolizine derivatives from α-picoline derivatives and nitroolefins.

Meng Gao1, Jun Tian, Aiwen Lei.   

Abstract

A reagent-free oxidative cyclization between α-picoline derivatives and nitroolefins has been developed. This approach, in which the nitro group acts as an internal oxidant, provides an extremely simple, efficient, and atom-economic way to construct heteroaromatic indolizine derivatives.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  green chemistry; indolizines; nitroolefins; oxidative cyclization; reagent-free; synthetic methods

Mesh:

Substances:

Year:  2014        PMID: 24782111     DOI: 10.1002/asia.201402096

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  1 in total

1.  Cu-Catalyzed Transannulation Reaction of Pyridotriazoles with Terminal Alkynes under Aerobic Conditions: Efficient Synthesis of Indolizines.

Authors:  V Helan; A V Gulevich; V Gevorgyan
Journal:  Chem Sci       Date:  2015-03       Impact factor: 9.825

  1 in total

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