The asymmetric reduction of ketones using chiral ammonium fluoride salts and silanes

DOI: 10.1016/S0040-4039(97)01445-7

Source and publish data:

Tetrahedron Letters p. 5857 - 5860 (1997)

Update date:2022-08-25

Topics:

Authors:

Drew, Mark D.

Lawrence, Nicholas J.

Watson, William

Bowles, Stephen A.

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

Article abstract of DOI:10.1016/S0040-4039(97)01445-7

Acelophenone and substituted arylalkyl ketones are reduced with moderate to good enantioselectivity by silanes bearing alkoxyl or siloxy groups and chiral ammonium fluoride salts derived from cinchona alkaloids.

Full text of DOI:10.1016/S0040-4039(97)01445-7

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

Sichuan WeiKeqi Biological Technology Co., Ltd.

website:https://www.weikeqi-biotech.com/en

Contact:86-028-81700200

Address:sichuan Chengdu Qingjiang Zhonglu 63号
HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou
Shanghai Xinda Pharmaceuticals Co., Ltd.

Contact:86-21-33692333-8008

Address:999 Linxian Road, Jinshan Industrial Park, Shanghai, China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China

Relevant to this article

Electrochemical Mechanism for Fullerene Formation in Plasma Arcs

Doi:10.1021/j100073a007
(1994)
Facile synthesis of iridium nanocrystals with well-controlled facets using seed-mediated growth

Doi:10.1021/ja505716v
(2014)
CuO nanostructures of variable shapes as an efficient catalyst for [3 + 2] cycloaddition of azides with terminal alkyne

Doi:10.1039/c6ra20725a
(2016)
Polyhalogenated Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acids

Doi:10.1021/acs.joc.1c01020
(2021)
Doi:10.1007/BF01381516
(1878)
A rhodium-grafted hydrotalcite as a highly efficient heterogeneous catalyst for 1,4-addition of organoboron reagents to α,β-unsaturated carbonyl compounds

Doi:10.1016/j.tetlet.2006.05.075
(2006)

Article Doi