NUCLEOPHILIC-ADDITION OF HIGHLY HINDERED AMINES TO ELECTRON-DEFICIENTACETYLENES

Authors
COSSU S DELUCCHI O DURR R
Citation
S. Cossu et al., NUCLEOPHILIC-ADDITION OF HIGHLY HINDERED AMINES TO ELECTRON-DEFICIENTACETYLENES, Synthetic communications, 26(24), 1996, pp. 4597-4601
Citations number
6
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
26
Issue
24
Year of publication
1996
Pages
4597 - 4601
Database
ISI
SICI code
0039-7911(1996)26:24<4597:NOHHAT>2.0.ZU;2-E
Abstract
Even the most highly hindered amines such as diisopropylamine, isoprop yl-t-butylamine, 2,2,6,6-tetramethylpiperidine, 4-oxo-2,2,6,6-tetramet hyl piperidine and hexamethyldisilazane react with electron-deficient alkynes to give the Michael addition products.