A General Non-Reductive Method for the Desulfenylation of 3-Indolyl Sulfides

DOI: 10.1016/S0040-4039(00)60345-3

Source and publish data:

Tetrahedron Letters p. 2059 - 2062 (1993)

Update date:2022-08-16

Topics:

Authors:

Hamel, Pierre

Zajac, Nicolas

Atkinson, Joseph G.

Girard, Yves

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

Article abstract of DOI:10.1016/S0040-4039(00)60345-3

In trifluoroacetic acid, in the presence of thiosalicyclic acid as a trapping agent, 3-indolyl sulfides bearing a wide variety of substituents are smoothly and rapidly desulfenylated to the corresponding 3-unsubstituted indoles.

Full text of DOI:10.1016/S0040-4039(00)60345-3

Products guided by the article

Product name:Methyl 1H-indole-2-carboxylate

Cas No:1202-04-6

R&D Labs maybe for 1202-04-6

Hangzhou JINLAN Pharm-Drugs Technology Co., Ltd

website:http://www.jlpharms.com

Contact:86-571-86982636

Address:Rm A606, Fuyi Center, jianqiao street
Dongguan Albiya Energy Science and Technology Co.,Ltd

Contact:+86-769-22181286

Address:Huanan Industial Park, Dongguan,China
Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
HangZhou HuaYe Chemical Technology Co.,Ltd

Contact:+86-13505815007

Address:hangzhou
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN

Relevant to this article

Application of the semi-pinacol rearrangement towards the generation of alkenyl-substituted quaternary carbon centres

Doi:10.1039/b611912c
(2006)
Electrochemical Polymerization of N-Trimethylsilylpyrrole and Other Substituted Pyrroles Which Contain Si or Ge Atom(s) in Their Monomer Structures

Doi:10.1246/bcsj.63.1716
(1990)
Doi:10.1016/S0020-1693(00)91948-0
(1980)
PREPARATION OF 2-VINYLCYCLOBUTANONES AND THEIR CONVERSION TO CYCLOPENTENONES

Doi:10.1016/S0040-4039(00)94015-2
(1983)
Diphenyl Diselenide Catalyzed Oxidative Degradation of Benzoin to Benzoic Acid

Doi:10.1055/s-0037-1611761
(2019)
Post-synthetic preparation of Sn-, Ti- and Zr-beta: A facile route to water tolerant, highly active Lewis acidic zeolites

Doi:10.1039/c3dt52972j
(2014)

Article Doi