Chiral thiourea as ligand for the asymmetric reduction of prochiral ketones

DOI: 10.1016/S0040-4039(97)00360-2

Source and publish data:

Tetrahedron Letters p. 2275 - 2278 (1997)

Update date:2022-08-11

Topics:

Authors:

Touchard, Francois

Gamez, Patrick

Fache, Fabienne

Lemaire, Marc

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(97)00360-2

The catalytic enantioselective reduction of prochiral ketones using a chiral thiourea as ligand is reported. Several metallic precursors were tested. e.e.'s up to 94% are obtained with a ruthenium complex.

Full text of DOI:10.1016/S0040-4039(97)00360-2

Products guided by the article

Product name:(R)-(+)-2-METHYL-1-PHENYL-1-PROPANOL

Cas No:14898-86-3

R&D Labs maybe for 14898-86-3

Mollt Biochem Co., Ltd(expird)

Contact:+86-21-38682181

Address:shanghai ,china
Chongqing Werlchem Fine Chemical Co. Ltd

Contact:+86-23-67521957

Address:NO.15,Fortune Road,Yubei District,401121,Chongqing,China
Anhui Hope-Chem Co., Ltd.

Contact:86-551-63540590

Address:No 1388 Furong Rd., Hefei, Anhui, China
SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China
Qingzhou Baibang import and export co.,Ltd

Contact:+86-536-3265899

Address:No.338, Tuoshan Road

Relevant to this article

Doi:10.1021/ja01280a003
(1937)
Anticoagulant activity of singlet oxygen released from a water soluble endoperoxide by thermal cycloreversion

Doi:10.1039/d1ra02569d
(2021)
Renewable hydrogen production by a mild-temperature steam reforming of the model compound acetic acid derived from bio-oil

Doi:10.1016/j.molcata.2011.12.006
(2012)
Engineering the Substrate Specificity of a Modular Polyketide Synthase for Installation of Consecutive Non-Natural Extender Units

Doi:10.1021/jacs.8b10521
(2019)
Natural coumarins. VII. Isolation and structure of a new coumarin, peuruthenicin, from Peucedanum ruthenicum M.B.

Doi:10.1002/jps.2600621133
(1973)
Improved process for the enantioselective hydrolysis of prochiral diethyl malonates catalyzed by pig liver esterase

Doi:10.1055/s-2005-871548
(2005)

Article Doi