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 |
| State | Published - 2001 |
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Keywords
- Monoselenophosphate
- Nitriles
- Selenocarboxamides
ASJC Scopus subject areas
- Organic Chemistry
Cite this
A convenient synthesis of selenocarboxamides from nitriles. / Kamiñski, R.; Glass, Richard S; Skowroñska, A.
In: Synthesis, No. 9, 2001, p. 1308-1310.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - A convenient synthesis of selenocarboxamides from nitriles
AU - Kamiñski, R.
AU - Glass, Richard S
AU - Skowroñska, A.
PY - 2001
Y1 - 2001
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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UR - http://www.scopus.com/inward/citedby.url?scp=0034929559&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0034929559
SP - 1308
EP - 1310
JO - Synthesis
JF - Synthesis
SN - 0039-7881
IS - 9
ER -