Process for the production of chiral unsaturated alcohols in hig

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters

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560113, C07C 702

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active

058862145

ABSTRACT:
The catalytic asymmetric hydrogenation of enol esters with a vinyllic or acetylenic substituent proceeds with extremely high enantioselectivity using a Rhodium-chiral bisphosphine catalyst. This is at variance with the hydrogenation of enol esters bearing a saturated substituent, which are hydrogenated with only marginal enantioselectivity under the same conditions.

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