A convenient synthesis of selenocarboxamides from nitriles

R. Kamiñski; R. S. Glass; A. Skowroñska

doi:10.1055/s-2001-15232

A convenient synthesis of selenocarboxamides from nitriles

R. Kamiñski, R. S. Glass, A. Skowroñska

Chemistry and Biochemistry

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

19 Scopus citations

Abstract

Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with monoselenophosphate in aqueous alcohol in 50-94% yield.

Original language	English (US)
Pages (from-to)	1308-1310
Number of pages	3
Journal	Synthesis
Issue number	9
DOIs	https://doi.org/10.1055/s-2001-15232
State	Published - Jan 1 2001

Keywords

Monoselenophosphate
Nitriles
Selenocarboxamides

ASJC Scopus subject areas

Catalysis
Organic Chemistry

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10.1055/s-2001-15232

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title = "A convenient synthesis of selenocarboxamides from nitriles",

abstract = "Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with monoselenophosphate in aqueous alcohol in 50-94% yield.",

keywords = "Monoselenophosphate, Nitriles, Selenocarboxamides",

author = "R. Kami{\~n}ski and Glass, {R. S.} and A. Skowro{\~n}ska",

year = "2001",

month = jan,

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doi = "10.1055/s-2001-15232",

language = "English (US)",

pages = "1308--1310",

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AU - Kamiñski, R.

AU - Glass, R. S.

AU - Skowroñska, A.

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Y1 - 2001/1/1

N2 - Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with monoselenophosphate in aqueous alcohol in 50-94% yield.

AB - Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with monoselenophosphate in aqueous alcohol in 50-94% yield.

KW - Monoselenophosphate

KW - Nitriles

KW - Selenocarboxamides

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JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 9

ER -

A convenient synthesis of selenocarboxamides from nitriles

Abstract

Keywords

ASJC Scopus subject areas

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