Nucleophilic and electrophilic additions to silylated ketenimines generated from imidothioesters

Article abstract of DOI:10.1080/10426509708545566

The reactivity of stable silylated N-phenyl ketenimines towards some nucleophilic (organometallics, alcohols, thiols) and electrophilic reagents (PhSCl) were studied. Imino-coumarines (via tandem nucleophilic-electrophilic additions with Peterson olefination) and new phenylthio-and silyl-substituted ketenimines have been prepared.

Full text of DOI:10.1080/10426509708545566

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Phosphorus, Sulfur, and Silicon
and the Related Elements
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Nucleophilic and Electrophilic
Additions to Silylated Ketenimines
Generated from Imidothioesters.
Christophe Fromont & Serge Masson
a Laboratoire de Chimie Moléculaire et Thio-organique ,
URA CNRS 480 ISMRA-Universté de Caen , F-14050 Caen,
France
b Laboratoire de Chimie Moléculaire et Thio-organique ,
URA CNRS 480 ISMRA-Universté de Caen , F-14050 Caen,
France
Published online: 17 Mar 2008.
To cite this article: Christophe Fromont & Serge Masson (1997) Nucleophilic and
Electrophilic Additions to Silylated Ketenimines Generated from Imidothioesters.,
Phosphorus, Sulfur, and Silicon and the Related Elements, 120:1, 397-398, DOI:
10.1080/10426509708545566
To link to this article: http://dx.doi.org/10.1080/10426509708545566
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