REACTION OF LANTHANIDE DERIVATIVES WITH VINYL BROMIDE IN THE PRESENCE OF COBALT CHLORIDE

DOI: 10.1007/BF00954395

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1543 (1983)

Update date:2022-08-10

Topics:

Authors:

Sigalov, A. B.

Rybakova, L. F.

Beletskaya, I. P.

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

Article abstract of DOI:10.1007/BF00954395

Full text of DOI:10.1007/BF00954395

Products guided by the article

Product name:Phenylethene

Cas No:100-42-5

R&D Labs maybe for 100-42-5

Zouping Mingxing Chemical Co.,Ltd.

website:http://www.zoutong.com.cn

Contact:86-543-2240068 2240067

Address:428 Daixi Third Road Zouping County Shandong Province China
Chemsky（shanghai）International Co.,Ltd.

Contact:0

Address:0
Nanjing Chemzam Pharmtech Co., Ltd.

Contact:+86-25-86462165,+86-13915979898

Address:C5-1，6 Maiyue Road，Maigaoqiao，Nanjing，Jiangsu，China
Sichuan WeiKeqi Biological Technology Co., Ltd.

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

Contact:86-028-81700200

Address:sichuan Chengdu Qingjiang Zhonglu 63号
Shanghai PotentPharm Science and Technology Co.,Ltd

Contact:86-021-51969655

Address:Unit B, Building 18, No.300, Chuantu Rd,Pudong District, Shanghai 201202, China

Relevant to this article

Salamo-type trinuclear and tetranuclear cobalt(II) complexes based on a new asymmetry Salamo-type ligand: Syntheses, crystal structures, and fluorescence properties

Doi:10.1080/00958972.2016.1168520
(2016)
Post-modification of a MOF through a fluorescent-labeling technology for the selective sensing and adsorption of Ag⁺ in aqueous solution

Doi:10.1039/c2dt30689a
(2012)
Synthesis and structures of gallaarsenes LGaAsGa(X)L featuring a Ga-As double bond

Doi:10.1039/c9dt03998h
(2019)
4-Aryloxybutenolides as "chiral aldehyde" equivalents: An efficient enantioselective synthesis of (+)-brefeldin A

Doi:10.1021/ja026438b
(2002)
Quinic acid derivatives and coumarin glycoside from the roots and stems of Erycibe obtusifolia

Doi:10.1016/j.phytol.2015.10.002
(2015)
Expanding Substrate Specificity of ω-Transaminase by Rational Remodeling of a Large Substrate-Binding Pocket

Doi:10.1002/adsc.201500239
(2015)

Article Doi