Unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates

Basavaiah, D. ; Pandiaraju, S. ; Krishnamacharyulu, M. (1996) Unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates Synlett, 1996 (8). pp. 747-748. ISSN 0936-5214

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Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-1996-5524

Abstract

An unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates with triethyl orthoacetate with a plausible mechanism has been described.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:The Johnson-Claisen Rearrangement; The Baylis-Hillman Reaction; Methyl 3-hydroxy-2-methylenealkanoates; (Z)- and (E)-alk-4-enoates
ID Code:85768
Deposited On:06 Mar 2012 04:43
Last Modified:06 Mar 2012 04:43

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