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ChemInform Abstract: Easy and General Method to Synthesize Chiral 2‐Hydroxy Acid Benzoates.

Victor S. Martı́n, Maria Teresa Nunez, Carlos Eugenio Tonn

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Abstract

Abstract The oxiranes (I), obtained by asymmetric epoxidation of the corresponding allylic alcohols, are selectively cleaved with benzoic acid (II) in the presence of titanium tetra(isopropoxide) to form the dihydroxy benzoates (III).

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What this paper is about

Abstract The oxiranes (I), obtained by asymmetric epoxidation of the corresponding allylic alcohols, are selectively cleaved with benzoic acid (II) in the presence of titanium tetra(isopropoxide) to form the dihydroxy benzoates (III).

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Available abstract

Abstract The oxiranes (I), obtained by asymmetric epoxidation of the corresponding allylic alcohols, are selectively cleaved with benzoic acid (II) in the presence of titanium tetra(isopropoxide) to form the dihydroxy benzoates (III).

Key concepts: Benzoates, Chemistry, Allylic rearrangement, Benzoic acid, Organic chemistry, Titanium, Medicinal chemistry, Catalysis

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ChemInform Abstract: Easy and General Method to Synthesize Chiral 2‐Hydroxy Acid Benzoates. — Research Paper | ScholarLens