Darstellung von η3-allyl-1-norbornyl-komplexen des nickels und palladiums

DOI: 10.1016/S0022-328X(96)87022-7

Source and publish data:

Journal of Organometallic Chemistry p. 83 - 85 (1996)

Update date:2022-08-04

Topics:

Authors:

Lehmkuhl, Herbert

Dimitrov, Vladimir

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

Article abstract of DOI:10.1016/S0022-328X(96)87022-7

[η³-Allyl-NiCl]₂ reacts at -78°C with 1-norLi (2) (1-nor = 1-norbornyl = bicyclo[2.2.1]heptane-1-yl) to give the highly unstable η³-allyl-Ni(1-nor) which decomposes rapidly under formation of nickel. The phosphane complexe

Full text of DOI:10.1016/S0022-328X(96)87022-7

Products guided by the article

Product name:(η(3)-allyl)(1-norbornyl)(triphenylphosphine)nickel

Cas No:179991-78-7

R&D Labs maybe for 179991-78-7

Xian Lyphar Biotech Co., Ltd.

Contact:0086-29-89196322

Address:North of the Fifth Keji Road, Hi-Tech Industrial Zone, Xi'an City, Shaanxi Province, China
Tianjin Tongde Biological Technology Co., Ltd.

Contact:86-22-23309138

Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
JenKem Technology Co., Ltd.

Contact:86-10-62983737; +86-10-51287608

Address:4/F Building C, 2 Shangdi Xinxi Road
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China

Relevant to this article

Synthesis and X-ray crystal structure of [Li(C₄H₈O)₄][Ni(2,4,6-Me₃C ₆H₂)₃]

Doi:10.1016/0277-5387(96)00056-3
(1996)
Chemistry of trichlorosilyl enolates. 1. New reagents for catalytic, asymmetric aldol additions

Doi:10.1021/ja9606539
(1996)
Octahydrogenated retinoic acid-conjugated glycol chitosan nanoparticles as a novel carrier of azadirachtin: Synthesis, characterization, and in vitro evaluation

Doi:10.1002/pola.26801
(2013)
beta-Dimethylaminoethyl ethers of substituted 2-benzylphenols.

Doi:10.1021/ja01169a018
(1949)
Introducing new phosphorus substituents in terminal phosphinidene complexes. An illustration with [(ethoxycarbonyl)phosphinidene]-, (tert-butoxyphosphinidene)-, and (fluorenylphosphinidene)pentacarbonyltungsten complexes

Doi:10.1021/om00098a017
(1988)
Studies on histaminergic compounds VIII. A new series of compounds showing H₁-antagonistic and H₂-agonistic properties; synthesis, in vitro pharmacology and structure-activity relationships

Doi:10.1016/0223-5234(87)90288-1
(1987)

Article Doi