REGIOSELECTIVITY OF NUCLEOPHILIC ADDITIONS TO TRICARBONYL5-2-METHYL-2,4-CYCLOHEXADIEN-1-YL>IRON(1+)PF6-: TEMPERATURE DEPENDENCE OF HYDRIDE REDUCTIONS

DOI: 10.1016/S0022-328X(00)80990-0

Source and publish data:

Journal of Organometallic Chemistry p. 91 - 104 (1981)

Update date:2022-08-02

Topics:

Authors:

Birch, Arthur J.

Stephenson, G. Richard

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

Article abstract of DOI:10.1016/S0022-328X(00)80990-0

Reduction of <(η⁵-CH3C6H6)Fe(CO)3>⁺PF6^- by NaBH4, LiBH4, LiEt3BH and KBu^s₃BH becomes less regioselective at lower temperatures.Regioselectivity of reduction by 9-BBN, however, improves as the temperat

Full text of DOI:10.1016/S0022-328X(00)80990-0

Products guided by the article

Product name:hexacarbonyl[2,6-di-[(2,3,4,5-η)-4-methyl-2,4-cyclohexadien-1-yl]-4-methylbenzeneamine]diiron(0)

Cas No:73623-52-6

R&D Labs maybe for 73623-52-6

TIANJIN ZHONGXIN CHEMTECH CO.,LTD.

Contact:86-022-66880623

Address:FINANCIAL STREET WEST BLK 7, #308, NO.52 XINCHENG WEST ROAD, TEDA, TIANJIN, P.R.CHINA
Chinese Peptide Company

Contact:86-571-86737118-8689

Address:No.69, 12 Street, HEDA, Hangzhou, Zhejiang, China
Rizhao Lanxing Chemical Indusrial Co.,Ltd

Contact:86-633-2616708

Address:NO.15 West road Shenglan, Lanshan district, Rizhao City
Chongqing Shuangfeng Chemical Co.,Ltd

Contact:+86-23-49850156

Address:No.663,xuanhua Rd,yongchuan,chongqing,China
Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China

Relevant to this article

Homosolvolysis

Doi:10.1039/P29800000260
(1980)
P(MeNCH₂CH₂)₃N: An efficient silylation catalyst

Doi:10.1021/ja961010w
(1996)
Alkylation of Pyrrolidine-2,5-dione with 2-(3,4-Dihydro-1-napthalenyl)ethyl-4-methylphenylsulphonates: A New and General Approach to 13-Azaequilenin Analogs

Doi:10.1081/SCC-120027232
(2004)
Substituent effect on the diastereoselectivity in the chelation-controlled radical reactions of γ-(p-substituted-benzyloxy)-α-methylene esters with alkyl iodides

Doi:10.1016/j.tet.2004.05.020
(2004)
Synthesis of a partial sequence of proinsulin using the A-chain of natural insulin. III. Synthesis of a peptide corresponding to positions 41-81 of bovine proinsulin

Doi:10.1246/bcsj.53.197
(1980)
Doi:10.1021/je60044a054
(1970)

Article Doi