Asymmetric iodoesterification of simple alkenes by concerto catalyst

Japanese researchers have succeeded in catalytic asymmetric iodoesterification from simple alkene substrates and carboxylic acids. Published in Angewandte Chemie International Edition on April 27, this new research, was accomplished by precisely controlling multiple interactions in a single catalytic reaction. This synthetic reaction is expected to contribute to the simplification of industrial processes and greater efficiency in optical active drug production.
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