Synthesis of primary-alkyl selenols and selenides from primary-alkyl thiols involving diphenyl sulfonium salts

Research output: Contribution to journalArticle

Abstract

Hexyl thiol has been transformed to hexyl selenol and related selenides and selenocyanate by substitution of the corresponding hexyldiphenylsulfonium tetrafluoroborate with selenium nucleophiles.
Original languageEnglish
Pages (from-to)2167-2168
Number of pages2
JournalChemical Communications
Issue number16
DOIs
Publication statusPublished - 28 Apr 2005

Fingerprint

Nucleophiles
Selenium
Sulfhydryl Compounds
Substitution reactions
Salts
diphenyl
selenocyanic acid
selenol

Cite this

@article{ab24078f4ec34f6b8235ae8512366046,
title = "Synthesis of primary-alkyl selenols and selenides from primary-alkyl thiols involving diphenyl sulfonium salts",
abstract = "Hexyl thiol has been transformed to hexyl selenol and related selenides and selenocyanate by substitution of the corresponding hexyldiphenylsulfonium tetrafluoroborate with selenium nucleophiles.",
author = "A. Krief and W. Dumont and M. Robert",
year = "2005",
month = "4",
day = "28",
doi = "10.1039/b418026g",
language = "English",
pages = "2167--2168",
journal = "Chem. Comm.",
issn = "1359-7345",
publisher = "The Royal Society of Chemistry",
number = "16",

}

TY - JOUR

T1 - Synthesis of primary-alkyl selenols and selenides from primary-alkyl thiols involving diphenyl sulfonium salts

AU - Krief, A.

AU - Dumont, W.

AU - Robert, M.

PY - 2005/4/28

Y1 - 2005/4/28

N2 - Hexyl thiol has been transformed to hexyl selenol and related selenides and selenocyanate by substitution of the corresponding hexyldiphenylsulfonium tetrafluoroborate with selenium nucleophiles.

AB - Hexyl thiol has been transformed to hexyl selenol and related selenides and selenocyanate by substitution of the corresponding hexyldiphenylsulfonium tetrafluoroborate with selenium nucleophiles.

UR - http://www.scopus.com/inward/record.url?scp=18544373897&partnerID=8YFLogxK

U2 - 10.1039/b418026g

DO - 10.1039/b418026g

M3 - Article

AN - SCOPUS:18544373897

SP - 2167

EP - 2168

JO - Chem. Comm.

JF - Chem. Comm.

SN - 1359-7345

IS - 16

ER -