ONE POT CONVERSION OF ALKYL HALIDES INTO THIOLS UNDER MILD CONDITIONS

DOI: 10.1016/S0040-4039(00)61913-5

Source and publish data:

Tetrahedron Letters p. 469 - 472 (1985)

Update date:2022-08-03

Topics:

Authors:

Molina, P.

Alajarin, M.

Vilaplana, M. J.

Katritzky, A. R.

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

Article abstract of DOI:10.1016/S0040-4039(00)61913-5

Alkyl halides are converted into the corresponding thiols in good yields at room temperature under neutral conditions by reaction with 1-(2-hydroxyethyl)-4,6-diphenylpyridine-2-thione.

Full text of DOI:10.1016/S0040-4039(00)61913-5

Products guided by the article

Product name:2(1H)-Pyridinethione, 1-(2-hydroxyethyl)-4,6-diphenyl-

Cas No:96185-26-1

R&D Labs maybe for 96185-26-1

Hubei Sibo Technology Co.,Ltd.

Contact:0715-6597222

Address:Pan Jia Wan fan Lake Chemical Industrial Park ,Xianning City, Hubei, China
BioBioPha Co., Ltd

Contact:+86-871-65217109

Address:132 Lanhei Road, Kunming Institute of Botany, Chinese Academy of Sciences
Taizhou YOJOY Chemical Co., Ltd.

Contact:13857143241

Address:Yangfu Industrial Park, Xianju, Zhejiang, P. R. China
HEZE KINGVOLT CHEMICAL CO., LTD

Contact:86-573-82118911

Address:Juancheng Industry Park
Shenzhen Hongyuan Import & Export Co., Ltd.

Contact:0755-26407171

Address:Shenzhen Hongyuan Chemical New Materials Technology Co., Ltd.

Relevant to this article

Synthesis of 1-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-5-benzyluracil and its amino analogue, new potent uridine phosphorylase inhibitors with high water solubility

Doi:10.1021/jm00145a023
(1985)
Synthesis of new antiinflammatory steroidal 20-carboxamides: (20R)- and (20S)-21-(N-substituted amino)-11β,17,20-trihydroxy-3,21-dioxo-1,4-pregnadiene

Doi:10.1021/jm00395a011
(1987)
Doi:10.1021/jo01068a056
(1961)
One-pot synthesis of 3-bromoimidazo[1,2-a]pyridine derivatives accompanied by dimethyl sulfoxide oxidation

Doi:10.1246/cl.2006.270
(2006)
Doi:10.1021/ja01463a045
(1961)
Doi:10.1039/jr9610004892
(1961)

Article Doi