CATALYTIC ENANTIOSELECTIVE ADDITION OF DIETHYLZINC TO ALDEHYDES: APPLICATION OF A NEW BICYCLIC CATALYSTS

DOI: 10.1016/S0957-4166(00)80167-6

Source and publish data:

Tetrahedron Asymmetry p. 637 - 640 (1993)

Update date:2022-08-11

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Authors:

Wallbaum, Sabine

Martens, Juergen

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Article abstract of DOI:10.1016/S0957-4166(00)80167-6

The optically active β-amino alcohol (1R,3R,5R)-3-(diphenylhydroxymethyl)-2-azabicyclo<3.3.0>octane (1R,3R,5R)-1 derived from a bicyclic proline analogue catalyzes the enantioselective addition of diethylzinc to various aldehydes.The resulting chiral seco

Full text of DOI:10.1016/S0957-4166(00)80167-6

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