Diastereo and Enantioselective Entry to β-Amino Esters by Hydride Reduction of Homochiral β-Enamino Esters.

DOI: 10.1016/0957-4166(94)80111-8

Source and publish data:

Tetrahedron Asymmetry p. 1455 - 1458 (1994)

Update date:2022-08-11

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Authors:

Cimarelli, Cristina

Palmieri, Gianni

Bartoli, Giuseppe

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Article abstract of DOI:10.1016/0957-4166(94)80111-8

The reduction of homochiral β-enamino esters 1 with sodium triacetoxyborohydride, which occurs with good diastereo- and enantioselectivity in the β-amino esters 2, is described.The procedure allows a straightforward preparation of compounds with known bio

Full text of DOI:10.1016/0957-4166(94)80111-8

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