Patterns of Nucleophilic Attack on Ethene Complexes of Ruthenium(II)

DOI: 10.1039/DT9810002112

Source and publish data:

Journal of the Chemical Society, Dalton Transactions p. 2112 - 2118 (1981)

Update date:2022-08-04

Topics:

Authors:

Stephenson, Martin

Mawby, Roger J.

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

Article abstract of DOI:10.1039/DT9810002112

Although reaction of with the nucleophile PMe2Ph at 308 K simply results in substitution of the ethene ligand, studies at lower temperatures reveal that the kinetically favoured product is the cation View More

Full text of DOI:10.1039/DT9810002112

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:[Ru(CO)Cl₂(NH₂CH₂Ph)(PMe₂Ph)2]

Cas No:80411-29-6

R&D Labs maybe for 80411-29-6

Changzhou Hopschain Chemical Co.,Ltd

website:http://www.hopschem.cn/products.html

Contact:86-519-85528066

Address:Room 710, Unit A, Xingbei Development Mansion, Tongjiang Road, Changzhou City,213000, China
Zhejiang Chemline International Co., Ltd.

Contact:+86-571-88062298

Address:Hengdian Industry Area, Dongyang, Zhejiang, China
WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
Beijing Cooperate Pharmaceutical Co.,Ltd

website:http://www.cooperate-pharm.com/

Contact:86-01060279497

Address:No.507,Building 4,Tianhua Street, Biomedicine industrial Base
Zhejiang Kangfeng Chemical Co.,LTD.

Contact:+86-579-86709687

Address:Xueshizhai Industrial Zone, Weishan Town,Dongyang City, Zhejiang Province ,China

Relevant to this article

Synthesis of pyrimidine acyclonucleosides

Doi:10.1002/jhet.5570180520
(1981)
Synthesis and anti-HIV activity of different sugar-modified pyrimidine and purine nucleosides

Doi:10.1021/jm00118a033
(1988)
A new synthesis of benzoporphyrins using 4,7-dihydro-4,7-ethano-2H-isoindole as a synthon of isoindole

Doi:10.1039/a803656j
(1998)
Synthesis, Conformation, and Complexation Behavior of 2,9,18,25-Tetraoxa-33,34,35,36-tetrakis(acyloxymethyl)<8.8>(1,4)naphthalenophanes

Doi:10.1021/ja00370a026
(1982)
PEPTIDES-XXXXIV. SYNTHESIS OF THE 105-117 FRAGMENT OF A LYSOZYME ANALOGUE

Doi:10.1016/S0040-4020(01)98918-5
(1981)
Doi:10.1021/ja00955a044
(1966)

Article Doi