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

Synasia Inc

Contact:17316303296

Address:240 Amboy Ave
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District
Shanghai Mintchem Development ., Ltd

Contact:0086 21 5190 8570

Address:R602,4#,89Nong, Mudan Road Pudong Shanghai China
Zhejiang Allied Chemical Co.,Ltd

Contact:18967038207

Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
Beijing Harmony Chemical Co., Ltd.

Contact:86-010-84956928

Address:Room 207, Jin feng he B building, No 8 Xin Jie Kou Wai Street, Xi Cheng District, Beijing,PRC. 10008

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