Formation and chemistry of the transient 17-electron compounds CpFe(CO)L· (L = PMe2Ph, PPh3)

DOI: 10.1016/S0022-328X(96)06623-5

Source and publish data:

Journal of Organometallic Chemistry p. 137 - 143 (1997)

Update date:2022-07-30

Topics:

Authors:

Kuksis, Inga

Baird, Micheal C.

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

Article abstract of DOI:10.1016/S0022-328X(96)06623-5

Hydride hydrogen atom abstraction from the 18-electron compounds CpFe(CO)LH (L = PMe₂Ph, PPh₃) by the trityl radical results in formation of the 17-electron species CpFe(CO)(PMe₂Ph)^· and (CpFe(CO)PPh₃

Full text of DOI:10.1016/S0022-328X(96)06623-5

Products guided by the article

Product name:(C₅H₅)Fe(CO)(P(CH₃)2C₆H₅)Br

Cas No:66139-52-4

R&D Labs maybe for 66139-52-4

Hangzhou Showland Technology Co., Ltd.

Contact:86-571-88920516

Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA
Aqua Chem Industry Co., Ltd

Contact:+86-515-88356562

Address:No.2, West Daqing Road, Yancheng, Jiangsu, China
MTT Pharma & Bio-technology Co.,Ltd(expird)

Contact:+86-21-58407925

Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
Yueyang Hudex Pharmaceuticals Ltd.

Contact:0730-8748800

Address:Wujiang Bridge，Yueyang Economy & Technology Development Zone
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang

Relevant to this article

Doi:10.1017/S1092852900017478
(1929)
Chiroptical properties of 2,2’-bioxirane

Doi:10.1002/chir.22814
(2018)
Reductive ring-opening reaction of 2,3-epoxy-1,4-butanediones with SbCl₃-Bu₄NI in the presence of Na₂S ₂O₃·5H₂O

Doi:10.1080/00397910500180121
(2005)
A Hydrazone-Based exo-Directing-Group Strategy for β C-H Oxidation of Aliphatic Amines

Doi:10.1002/anie.201600912
(2016)
Catalytic Cyclization of o-Alkynyl Phenethylamines via Osmacyclopropene Intermediates: Direct Access to Dopaminergic 3-Benzazepines

Doi:10.1002/anie.201505782
(2015)
Use of Samarium Diiodide as an Alternative to Sodium/Mercury Amalgam in the Julia-Lythgoe Olefination

Doi:10.1021/jo00115a041
(1995)

Article Doi