FRE RADICAL SUBTITUTION REACTIONS OF PHENYLACETYLENE DERIVATIVES BY AN ADDITION-ELIMINATION MECHANISM

DOI: 10.1016/S0040-4039(00)84827-3

Source and publish data:

Tetrahedron Letters p. 3479 - 3482 (1986)

Update date:2022-08-11

Topics:

Authors:

Russell, Glen A.

Ngoviwatchai, Preecha

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

Article abstract of DOI:10.1016/S0040-4039(00)84827-3

Phenylacetylenes (PhC<*>CQ with Q=PhSO2, I, SPh, Bu3Sn PhC<*>CHg) undergo free radical chain substitution reactions with RHgCl, R2Hg, (EtO)2P(O)HgCl, (PhS)2Hg or (PhSO2)2Hg.The relative reactivities of PhC<*>CQ towards c-C6H11 ^. are Q = PhSO2 (

Full text of DOI:10.1016/S0040-4039(00)84827-3

Products guided by the article

Product name:1-PHENYL-1-HEXYNE

Cas No:1129-65-3

R&D Labs maybe for 1129-65-3

Anhui Asahikasei Chemical Co., Ltd

Contact:86-551-4259770

Address:No. 88 Linquan Road Hefei Anhui China
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park
Jinan Hongfangde Pharmatech Co.,Ltd

Contact:86-531-88870908

Address:F Bldg. West Unit North Area of Univ. Tech. Garden Xinyu Rd. Jinan New & High Tech Industry Development Zone Shandong, China
Shanghai Dynamic Industrial Co.,Ltd.

website:http://www.shdynamic.com

Contact:86-021 3392 6680

Address:Room 805 Information Tower, No.1403 Minsheng Road, Pudong New Area, Shanghai 200135, P. R. China
Shanghai agrotree chemical co.,ltd.

Contact:+86-21-50117563

Address:Room 8A,liangfeng building,No.8 dongfang RD.pudong,shanghai,China

Relevant to this article

The synergistic catalysis effect within a dinuclear nickel complex for efficient and selective electrocatalytic reduction of CO₂ to CO

Doi:10.1039/c7gc03451b
(2018)
The Induction Period and Novel Active Species in Zn(OAc)₂ Catalyzed Synthesis of Aromatic Carbamates

Doi:10.1007/s10562-017-2055-z
(2017)
A Model for the Active Sites of Oxo-Transfer Molybdoenzymes: Reactivity, Kinetics, and Catalysis

Doi:10.1021/ja00290a030
(1985)
Concentration and characterization of a triosekinase from liver. On the biochemistry of fructose metabolism. III.

Doi:10.1515/bchm2.1961.324.1.88
(1961)
Remarks on the Mechanism of Ethylene Formation from Methyl Alcohol

Doi:10.1039/c39860000009
(1986)
EVIDENCE OF STABLE HYDROGEN-BONDED IONS DURING ISOMERZATION OF HEXOSES IN ALKALI

Doi:10.1016/0008-6215(89)84020-0
(1989)

Article Doi