Regioselective Synthesis of Highly Functionalized Biaryls through Carbanion Induced Ring Transformation of 2H-Pyran-2-ones

Ram, Vishnu Ji ; Saxena, Abhishek Shanker ; Goel, Atul (2002) Regioselective Synthesis of Highly Functionalized Biaryls through Carbanion Induced Ring Transformation of 2H-Pyran-2-ones Synlett, 2002 (9). pp. 1491-1492. ISSN 0936-5214

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Official URL: http://doi.org/10.1055/s-2002-33538

Related URL: http://dx.doi.org/10.1055/s-2002-33538

Abstract

An expedient synthesis of highly functionalized unsymmetrical biaryls 3 of which one of the two phenyl rings substituted with carbomethoxy, amino and nitrile functionalities is described and illustrated by carbanion induced ring transformation of 6-aryl-3-carbomethoxy-4-methylsulfanyl-2H-pyran-2-one 1 using malononitrile 2 as a source of carbanion in moderate yield.

Item Type:Article
Source:Copyright of this article belongs to Georg Thieme Verlag.
Keywords:Biaryls; 2h-pyran-2-one; Malononitrile; Biaryls; Carb­anion; Ring Transformation.
ID Code:117896
Deposited On:06 May 2021 05:47
Last Modified:06 May 2021 05:47

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