REGIO- AND STEREO-CHEMISTRY IN ALLYLATION OF ARYL GRINARD REAGENTS CATALYZED BY PHOSPHINE-NICKEL AND -PALLADIUM COMPLEXES

DOI: 10.1016/0022-328X(85)87380-0

Source and publish data:

Journal of Organometallic Chemistry p. 359 - 374 (1985)

Update date:2022-08-04

Topics: Allylation Catalyzed Regiochemistry

Authors:

Hayashi, Tamio

Konishi, Mitsuo

Yokota, Kan-Ichi

Kumada, Makoto

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

Article abstract of DOI:10.1016/0022-328X(85)87380-0

Nickel and palladium complexes with the 1,1'-bis(diphenylphosphino)ferrocene ligand effectively catalyze regioselective cross-coupling of allylic ethers such as 1- or 3-methyl-2-propenyl silyl ethers with aryl-Grinard reagents, where the nickel catalyst l

Full text of DOI:10.1016/0022-328X(85)87380-0

Products guided by the article

Product name:Pd(CH₃CHCHCH₂)(Fe(C₅H₄(P(C₆H₅)2))2)⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Pd(CH₃CHCHCH₂)(Fe(C₅H₄(P(C₆H₅)2))2)]B(C₆H₅)4

Cas No:98047-80-4

R&D Labs maybe for 98047-80-4

Yicheng Goto Pharmaceuticals Co.,Ltd.

Contact:+86 710 3423122

Address:5th Floor,East Gate of Building #2,Servo-Industrial Park,1st Qilin Road,Xiangyang,Hubei,China
Suzhou Health Chemicals Co., Ltd.

website:http://www.healthchems.com

Contact:13776257979

Address:No. 338, Jingang Avenue,
Shanghai FWD Chemicals ltd

website:http://www.fwdchem.com

Contact:86-21-54450828

Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai
ZHEJIANG JIANYE CHEMICAL CO.,LTD.

Contact:86-571-64149273,64149234

Address:No. 48, Fuxi Road, Meicheng Town
QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071

Relevant to this article

INFLUENCE OF PHENOL ACIDITY AND SOLVENT POLARITY WITH PHENOL-RETINAL SCHIFF BASE HYDROGEN BONDS-THERMODYNAMIC PARAMETERS OF BOND FORMATION AND PROTON TRANSFER

Doi:10.1016/0022-2860(87)85064-0
(1987)
Total Synthesis of Sericenine

Doi:10.1021/jo00222a024
(1985)
Chemical constituents of the lichen, Candelaria concolor: A complete NMR and chemical degradative investigation

Doi:10.1080/14786410802682536
(2009)
Stereoselectivity in the cyclisation of photoinduced electron transfer (PET) generated cyclic α -amino radicals: First general stereoselective entry to 1-azabicyclo (m:n:o) alkane systems

Doi:10.1016/S0040-4039(00)79035-6
(1992)
Chemistry of Insect Antifeedants from Azadirachta indica, Part 14: Absolute Configuration of Azadirachtin

Doi:10.1039/c39920001304
(1992)
On the factors that affect the mode of cyclization of α-silyl radicals: A method for angular hydroxymethylation by the 5-exo cyclization

Doi:10.1016/S0040-4039(00)60996-6
(1992)

Article Doi