Literature DB >> 22765306

A novel strategy for the synthesis of 3-(N-heteryl)pyrrole derivatives.

Alexander F Khlebnikov1, Maria V Golovkina, Mikhail S Novikov, Dmitry S Yufit.   

Abstract

A flexible approach to unknown 1-(1H-pyrrol-3-yl)pyridinium salts with selective control of the substitution patterns, by the reaction of pyridinium ylides with 2H-azirines, is disclosed. 3-(Pyridinium-1-yl)pyrrolides, a new type of stable ylide, were prepared from these salts in high yields by treatment with base. Atmospheric-pressure hydrogenation of the ylides with Adams' catalyst lead to 1-(pyrrol-3-yl)piperidines in good yields.

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Year:  2012        PMID: 22765306     DOI: 10.1021/ol3016594

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Formation of diverse polycyclic spirooxindoles via three-component reaction of isoquinolinium salts, isatins and malononitrile.

Authors:  Jing Sun; Guo-Liang Shen; Ying Huang; Chao-Guo Yan
Journal:  Sci Rep       Date:  2017-01-20       Impact factor: 4.379

2.  Investigation on the reactivity of α-azidochalcones with carboxylic acids: Formation of α-amido-1,3-diketones and highly substituted 2-(trifluoromethyl)oxazoles.

Authors:  Kandasamy Rajaguru; Arumugam Mariappan; Rajendran Suresh; Periasamy Manivannan; Shanmugam Muthusubramanian
Journal:  Beilstein J Org Chem       Date:  2015-10-29       Impact factor: 2.883

  2 in total

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