Enantioselective catalysis .112. New chiral tertiary alcohols on the basis of deltacyclanes as precursors for hydroperoxides

Brunner, Henri and Reimer, A. (1997) Enantioselective catalysis .112. New chiral tertiary alcohols on the basis of deltacyclanes as precursors for hydroperoxides. BULLETIN DES SOCIETES CHIMIQUES BELGES, 106 (5). pp. 267-272. ISSN 0037-9646

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Abstract

Norbornadiene was reacted with 2-methyl-3-butin-2-ol 1 in an enantioselective homo Diels-Alder reaction to yield the deltacyclene 2 with 92% ee. 2 was hydrogenated stereoselectively to give the enantiomerically pure, deltacyclane-based tertiary alcohol 3, a candidate for conversion into an optically active hydroperoxide for enantioselective oxidation reactions.

Item Type: Article
Uncontrolled Keywords: DIELS-ALDER REACTION; ASYMMETRIC EPOXIDATION; SYSTEM
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Prof. Dr. Henri Brunner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 09 May 2023 06:42
Last Modified: 09 May 2023 06:42
URI: https://pred.uni-regensburg.de/id/eprint/50839

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