Synthesis of Novel Chiral Diazole Ligands for Enantioselective Addition of Diethylzinc to Benzaldehyde

DOI: 10.1016/0957-4166(95)00352-P

Source and publish data:

Tetrahedron Asymmetry p. 2665 - 2668 (1995)

Update date:2022-08-16

Topics:

Authors:

Kotsuki, Hiyoshizo

Hayakawa, Hiroyuki

Wakao, Masahiro

Shimanouchi, Tomoyasu

Ochi, Masamitsu

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

Article abstract of DOI:10.1016/0957-4166(95)00352-P

A variety of chiral pyrazole and imidazole derivatived ligands have been prepared under high pressure conditions and their catalytic efficiency in the enantioselective addition of diethylzinc to benzaldehyde has been examined.

Full text of DOI:10.1016/0957-4166(95)00352-P

Products guided by the article

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

Cas No:1565-74-8

R&D Labs maybe for 1565-74-8

Chongqing Yawei Fine Chemical Co.,Ltd

Contact:0086-23-62849407

Address:Ziyou village, Nanquan town, Banan district, Chongqing China
Ningbo Bichem Pharmaceutical Co.,Ltd

Contact:18957868060 057487816388

Address:ningbo
KindChem Co.,Ltd,

Contact:+86-25-85281586

Address:13F,Bld2#,South of Longpan Road
Shanghai Micro-mega Industry Co., Ltd.

Contact:0086-21-34628682;57153848

Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
Santow Laboratory Limited

Contact:+86-371-55981030

Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan

Relevant to this article

Recent studies on In₂S₃ containing oxygen thin films

Doi:10.1016/S0038-1098(02)00099-6
(2002)
Doi:10.1016/S0022-328X(00)87687-1
(1968)
Photocatalytic Activation of C-H Bonds by Spatially Controlled Chlorine and Titanium on the Silicate Layer

Doi:10.1021/acscatal.9b01284
(2019)
Synthesis and multicolor upconversion of Tm³⁺/Er³⁺/Yb³⁺ doped Na (Y_1.5Na_0.5) F₆ single-crystal nanorods

Doi:10.1016/j.jallcom.2009.12.133
(2010)
Mechanistic, kinetic and electroanalytical aspects of quinone-hydroquinone redox system in N-alkylimidazolium based room temperature ionic liquids

Doi:10.1016/j.electacta.2012.07.059
(2012)
Br?nsted Basicities and Nucleophilicities of N-Heterocyclic Olefins in Solution: N-Heterocyclic Carbene versus N-Heterocyclic Olefin. Which Is More Basic, and Which Is More Nucleophilic?

Doi:10.1021/acs.joc.0c02838
(2021)

Article Doi