
Tetrahedron p. 6385 - 6402 (1998)
Update date:2022-08-03
Topics:
Lutz, Christian
Lutz, Volker
Knochel, Paul
Chiral 1,3- and 1,4- aminoalcohols were prepared by the addition of functionalized dialkylzincs to 1,3-aliphatic and 1,4-unsaturated aminoaldehydes with good to excellent enantioselectivity. Syn- or anti-1,2- aminoalcohols are stereoselectively obtained by asymmetric addition of dialkylzincs to α-aminoaldehydes depending on the choice of the chiral catalyst. A chelate controlled addition is observed if less than stoichiometric amounts of Ti(Oi-Pr)4 are used.
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Doi:10.1016/S0040-4039(98)00936-8
(1998)Doi:10.1021/jm00327a029
(1965)Doi:10.1080/00397919808004296
(1998)Doi:10.1016/S0008-6215(98)00062-7
(1998)Doi:10.3390/molecules24244581
(2019)Doi:10.1016/S0040-4039(98)01096-X
(1998)