Nucleophilic addition of highly hindered amines to electron-deficient acetylenes

Article abstract of DOI:10.1080/00397919608004784

Even the most highly hindered amines such as diisopropylamine, isopropyl-t-butylamine, 2,2,6,6-tetramethylpiperidine, 4-oxo-2,2,6,6-tetramethyl piperidine and hexamethyldisilazane react with electron-deficient alkynes to give the Michael addition products

Full text of DOI:10.1080/00397919608004784

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Nucleophilic Addition of Highly
Hindered Amines to Electron-
Deficient Acetylenes
Sergio Cossu a , Ottorino De Lucchi a & Richard Durr
a
a Dipartimento di Chimica , Università Cá Foscari di
Venezia, Dorsoduro , 2137 I-30123, Venezia, Italy
Published online: 21 Aug 2006.
To cite this article: Sergio Cossu , Ottorino De Lucchi & Richard Durr (1996)
Nucleophilic Addition of Highly Hindered Amines to Electron-Deficient Acetylenes,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 26:24, 4597-4601, DOI: 10.1080/00397919608004784
To link to this article: http://dx.doi.org/10.1080/00397919608004784
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