Application of chiral cyclic diols to asymmetric alkylation

DOI: 10.1016/0040-4039(92)88062-A

Source and publish data:

Tetrahedron Letters p. 247 - 250 (1992)

Update date:2022-09-26

Topics:

Authors:

Kato, Keisuke

Suemune, Hiroshi

Sakai, Koyoshi

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

Article abstract of DOI:10.1016/0040-4039(92)88062-A

Chiral cyclic (6- or 7-membered ring) diols were found to be excellent chiral auxiliaries for asymmetric alkylation of cyclic (or acyclic) β-keto esters.

Full text of DOI:10.1016/0040-4039(92)88062-A

Products guided by the article

Product name:(Z)-3-((1R,2R)-2-Hydroxy-cycloheptyloxy)-2-methyl-but-2-enoic acid ethyl ester

Cas No:139616-50-5

R&D Labs maybe for 139616-50-5

GN chemicals co.,ltd

Contact:86 311 85902108 / 85902109

Address:room 1001-1005 ,huanghe Road ,shijiazhuang ,China
Jiangxi Dongxu Chemical Science & Technology Co.,Ltd

Contact:+86-791-86899381

Address:Nanchang, Jiangxi, China
shijiazhuang baisheng chem co.; ltd

Contact:86-0311-80790826

Address:shijiazhuang hebei
Shandong Jincheng Zhonghua Bio-pharmaceutical Co.,Ltd

Contact:+86-533-5415882

Address:Zichuan Economic Development Zone,Zibo City,Shandong Province,China
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China

Relevant to this article

A highly diastereoselective total synthesis of (±)-heritonin and (±)-heritol

Doi:10.1016/j.tet.2012.07.020
(2012)
Palladium-catalyzed substitution of (coumarinyl)methyl acetates with C-, N-, and S-nucleophiles

Doi:10.3762/bjoc.8.133
(2012)
An asymmetric synthesis of a chiral sulfone acid with concomitant hydrolysis and oxidation to enable the preparation of a glucokinase activator

Doi:10.1021/op300139g
(2012)
Electrochemical studies of nickel complexes containing phosphorus(III) ligands and their related Ziegler catalysts

Doi:10.1016/0022-328X(89)87220-1
(1989)
Synthesis and optical properties of phenylene-containing oligoacenes

Doi:10.1021/ja3043883
(2012)
Access to Unsaturated Chiral Expoxides. I: Bisallylic Chiral Expoxides. Application to the Synthesis of Lepidopteran Pheromones.

Doi:10.1016/S0040-4020(01)89006-2
(1992)

Article Doi