ChemInform Abstract: Enantioselective Reduction of Ketones in Optically Active Host Compounds with a BH3-Ethylenediamine Complex in the Solid State.

F. TODA; K. MORI

doi:10.1002/chin.199010105

ChemInform Abstract: Enantioselective Reduction of Ketones in Optically Active Host Compounds with a BH3-Ethylenediamine Complex in the Solid State.

ChemInform ◽

10.1002/chin.199010105 ◽

1990 ◽

Vol 21 (10) ◽

Author(s):

F. TODA ◽

K. MORI

Keyword(s):

Solid State ◽

Optically Active ◽

Enantioselective Reduction ◽

Ethylenediamine Complex ◽

Reduction Of Ketones

Download Full-text

Enantioselective reduction of ketones in optically active host compounds with a BH3–ethylenediamine complex in the solid state

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39890001245 ◽

1989 ◽

pp. 1245-1246 ◽

Cited By ~ 25

Author(s):

Fumio Tada ◽

Koji Mori

Keyword(s):

Solid State ◽

Optically Active ◽

Enantioselective Reduction ◽

Ethylenediamine Complex ◽

Reduction Of Ketones

Download Full-text

Enantioselective Reduction of Ketones with Sodium Borohydride, Catalyzed by Optically Active(β-Oxoaldiminato)cobalt(II) Complexes

Angewandte Chemie International Edition in English ◽

10.1002/anie.199521451 ◽

1995 ◽

Vol 34 (19) ◽

pp. 2145-2147 ◽

Cited By ~ 106

Author(s):

Takushi Nagata ◽

Kiyotaka Yorozu ◽

Tohru Yamada ◽

Teruaki Mukaiyama

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Enantioselective Reduction ◽

Reduction Of Ketones

Download Full-text

ChemInform Abstract: ENANTIOSELECTIVE REDUCTION OF KETONES WITH OPTICALLY ACTIVE 2,2′-DIAMINO-6,6′-DIMETHYLBIPHENYL-LITHIUM ALUMINUM HYDRIDE COMPLEX

Chemischer Informationsdienst ◽

10.1002/chin.198010129 ◽

1980 ◽

Vol 11 (10) ◽

Author(s):

H. SUDA ◽

M. MOTOI ◽

M. FUJII ◽

S. KANOH ◽

H. YOSHIDA

Keyword(s):

Lithium Aluminum Hydride ◽

Aluminum Hydride ◽

Optically Active ◽

Lithium Aluminum ◽

Enantioselective Reduction ◽

Hydride Complex ◽

Reduction Of Ketones

Download Full-text

Enantioselective reduction of ketones with optically active 2,2′-diamino-6,6′-dimethylbiphenyl-lithium aluminum hydride complex

Tetrahedron Letters ◽

10.1016/s0040-4039(01)86650-8 ◽

1979 ◽

Vol 20 (47) ◽

pp. 4565-4568 ◽

Cited By ~ 12

Author(s):

Hiroshi Suda ◽

Masatoahi Motoi ◽

Masatoshi Fujii ◽

Shigeyoshi Kanoh ◽

Hiroshi Yoshida

Keyword(s):

Lithium Aluminum Hydride ◽

Aluminum Hydride ◽

Optically Active ◽

Lithium Aluminum ◽

Enantioselective Reduction ◽

Hydride Complex ◽

Reduction Of Ketones

Download Full-text

Enantioselective Reduction of Ketones with “Designer Cells” at High Substrate Concentrations: Highly Efficient Access to Functionalized Optically Active Alcohols

Angewandte Chemie International Edition ◽

10.1002/anie.200503394 ◽

2006 ◽

Vol 45 (34) ◽

pp. 5677-5681 ◽

Cited By ~ 134

Author(s):

Harald Gröger ◽

Francoise Chamouleau ◽

Nicolas Orologas ◽

Claudia Rollmann ◽

Karlheinz Drauz ◽

...

Keyword(s):

Optically Active ◽

High Substrate ◽

Enantioselective Reduction ◽

Highly Efficient ◽

Efficient Access ◽

Substrate Concentrations ◽

Reduction Of Ketones

Download Full-text

Enantioselective reduction of ketones in inclusion complexes with cyclomaltoheptaose in the solid state: acceleration of the reaction by ultrasound

Carbohydrate Research ◽

10.1016/0008-6215(89)85196-1 ◽

1989 ◽

Vol 192 ◽

pp. 363-365 ◽

Cited By ~ 11

Author(s):

Fumio Toda ◽

Tatsuya Shigemasa

Keyword(s):

Solid State ◽

Inclusion Complexes ◽

Enantioselective Reduction ◽

Reduction Of Ketones

Download Full-text

ChemInform Abstract: Enantioselective Reduction of Ketones with Sodium Borohydride, Catalyzed by Optically Active (β-Oxoaldiminato)cobalt(II) Complexes.

ChemInform ◽

10.1002/chin.199604056 ◽

2010 ◽

Vol 27 (4) ◽

pp. no-no

Author(s):

T. NAGATA ◽

K. YOROZU ◽

T. YAMADA ◽

T. MUKAIYAMA

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Enantioselective Reduction ◽

Reduction Of Ketones

Download Full-text

Enantioselective reduction of ketones with NaBH4/diglyme possibly catalysed by trialkyl borate: optically active sec-alcohols from prochiral ketones with catalytic (−)-menthol: autocatalysis option

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2004.11.078 ◽

2005 ◽

Vol 16 (4) ◽

pp. 751-754 ◽

Cited By ~ 6

Author(s):

Sosale Chandrasekhar ◽

Raghunandan Hota

Keyword(s):

Optically Active ◽

Enantioselective Reduction ◽

Prochiral Ketones ◽

Reduction Of Ketones

Download Full-text

ChemInform Abstract: Enantioselective Reduction of Ketones. Examination of Bifunctional Ligands.

ChemInform ◽

10.1002/chin.199928033 ◽

2010 ◽

Vol 30 (28) ◽

pp. no-no

Author(s):

Mukund P. Sibi ◽

Gregory R. Cook ◽

Pingrong Liu

Keyword(s):

Enantioselective Reduction ◽

Bifunctional Ligands ◽

Reduction Of Ketones

Download Full-text

ChemInform Abstract: Enantioselective Reduction of Ketones (I) on Sterically-Controlled Lanthanoid(III) Complexes.

ChemInform ◽

10.1002/chin.198930100 ◽

1989 ◽

Vol 20 (30) ◽

Author(s):

H. OKAWA ◽

T. KATSUKI ◽

M. NAKAMURA ◽

N. KUMAGAI ◽

Y. SHUIN ◽

...

Keyword(s):

Enantioselective Reduction ◽

Reduction Of Ketones

Download Full-text