Reacción #1756877

ord-58186860048248e8a6736e84b4cbf52b

Ecuación de reacción

O=C1CCN(C(=O)OCc2ccccc2)c2ccccc21
1-benzyloxycarbonyl-4-oxo-1,2,3,4-tetrahydroquinoline
Cc1ccc(S(=O)(=O)N[C@@H](c2ccccc2)[C@@H](N)c2ccccc2)cc1
(S,S)-TsDPEN
→
O=C(OCc1ccccc1)N1CC[C@H](O)c2ccccc21
(4S)-1-benzyloxycarbonyl-4-hydroxy-1,2,3,4-tetrahydroquinoline
Rendimiento 86.2%

Reactantes

O=C1CCN(C(=O)OCc2ccccc2)c2ccccc21
1-benzyloxycarbonyl-4-oxo-1,2,3,4-tetrahydroquinoline
Cc1ccc(S(=O)(=O)N[C@@H](c2ccccc2)[C@@H](N)c2ccccc2)cc1
(S,S)-TsDPEN
—
[RuCl2(benzene)]2

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

1-benzyloxycarbonyl-4-oxo-1,2,3,4-tetrahydroquinoline (281 mg), [RuCl2(benzene)]2 (25.0 mg) and (S,S)-TsDPEN (73.3 mg) were treated in the same manner as Example 4 to give 244 mg of (4S)-1-benzyloxycarbonyl-4-hydroxy-1,2,3,4-tetrahydroquinoline (optical purity: 97% ee, yield: 86%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07989627B2uspto-grants-2011_08