Literature DB >> 34414516

An efficient domino strategy for synthesis of 3-substituted 4-oxo-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine derivatives in water.

Xiaopeng Yang1, Chunmei Li1,2, Furen Zhang3, Chenze Qi4.   

Abstract

A strategy for catalyst-free domino reaction of 4-aminopyridin-2(1H)-ones, arylglyoxal hydrates and different 1,3-dicarbonyl compounds in water has been established. The mild and efficient procedure afforded pyrrolo[3,2-c]pyridine derivatives with 76-94% yields after simple crystallization. The present procedure shows promising characteristics, such as readily available starting materials, the use of water as reaction media, simple and efficient one-pot operation, and avoiding the need for any hazardous or expensive catalysts.
© 2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Entities:  

Keywords:  Domino strategy; Pyrrolo[3,2-c]pyridine; Synthesis; Water

Mesh:

Substances:

Year:  2021        PMID: 34414516     DOI: 10.1007/s11030-021-10294-4

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  20 in total

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3.  An efficient one-pot synthesis of functionalized chromeno[4,3-b]pyridine derivatives under catalyst-free conditions.

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6.  Highly enantioselective construction of spiro[4H-pyran-3,3'-oxindoles] through a domino Knoevenagel/Michael/cyclization sequence catalyzed by cupreine.

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Journal:  Org Lett       Date:  2010-07-16       Impact factor: 6.005

7.  Enone-alkyne reductive coupling: a versatile entry to substituted pyrroles.

Authors:  Benjamin B Thompson; John Montgomery
Journal:  Org Lett       Date:  2011-06-09       Impact factor: 6.005

8.  Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles.

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Journal:  Acc Chem Res       Date:  2011-07-29       Impact factor: 22.384

9.  Base-promoted transannulation of heterocyclic enamines and 2,3-epoxypropan-1-ones: regio- and stereoselective synthesis of fused pyridines and pyrroles.

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10.  Enantioselective Construction of Tetrahydroquinolin-5-one-Based Spirooxindole Scaffold via an Organocatalytic Asymmetric Multicomponent [3 + 3] Cyclization.

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  1 in total

1.  One-pot multi-component synthesis of novel chromeno[4,3-b]pyrrol-3-yl derivatives as alpha-glucosidase inhibitors.

Authors:  Malihe Karami; Alireza Hasaninejad; Hossein Mahdavi; Aida Iraji; Somayeh Mojtabavi; Mohammad Ali Faramarzi; Mohammad Mahdavi
Journal:  Mol Divers       Date:  2021-10-25       Impact factor: 3.364

  1 in total

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