Asymmetric synthesis of chiral vinylic epoxides and α-hydroxy-β,γ-unsaturated esters via (-)-menthol based auxiliary and enzymatic resolution respectively 1

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Abstract

Using (-)-menthol as an auxiliary, three chiral vinylic epoxides have been synthesised from the corresponding glycidic esters via α-hydroxy-β,γ-unsaturated esters.Enzymatic resolution of α-acetoxy-β,γ-unsaturated esters using PLAP leads to optically active α-hydroxy-β,γ-unsaturated esters. Copyright © 1996 Elsevier Science Ltd.

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Vankar, P. S., Bhattacharya, I., & Vankar, Y. D. (1996). Asymmetric synthesis of chiral vinylic epoxides and α-hydroxy-β,γ-unsaturated esters via (-)-menthol based auxiliary and enzymatic resolution respectively 1. Tetrahedron Asymmetry, 7(6), 1683–1694. https://doi.org/10.1016/0957-4166(96)00202-9

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