THE STEREOSELECTIVE REDUCTION OF α-AMINODEOXYBENZOIN DERIVATIVES WITH SODIUM BOROHYDRIDE

DOI: 10.1016/S0040-4039(00)87253-6

Source and publish data:

Tetrahedron Letters p. 2033 - 2036 (1982)

Update date:2022-08-02

Topics: sodium borohydride Reduction Stereoselective

Authors:

Alcaide, Benito

Escobar, Gerardo

Gonzalez-Simo, Jose L.

Lopez-Mardomingo, Carmen

Perez-Ossorio, Rafael

Plumet, Joaquin

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Article abstract of DOI:10.1016/S0040-4039(00)87253-6

Total stereoselectivity is observed in the sodium borohydride reduction of α-aminodeoxybenzoins and their hydrochlorides in various hydroxylic solvents.RS-SR isomer (erythro) was the only aminoalcohol obtained.

Full text of DOI:10.1016/S0040-4039(00)87253-6

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