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

A. Krief; W. Dumont; M. Robert

doi:10.1039/b418026g

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

A. Krief, W. Dumont, M. Robert

Unit of organic chemistry

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	2167-2168
Number of pages	2
Journal	Chemical Communications
Issue number	16
DOIs	https://doi.org/10.1039/b418026g
Publication status	Published - 28 Apr 2005

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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 = apr,

day = "28",

doi = "10.1039/b418026g",

language = "English",

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journal = "Chemical Communications",

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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.

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U2 - 10.1039/b418026g

DO - 10.1039/b418026g

M3 - Article

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SP - 2167

EP - 2168

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

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

Abstract

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