Silylated β-enaminones as precursors in the regioselective synthesis of silyl pyrazoles
Silyl β-enaminones have been synthesized by reductive cleavage of 5-silyl, 3-, 4- and 5-silylmethylisoxazoles.These versatile synthons bearing different silyl groups in various positions of the enaminoketonic system are of great interest in the regioselective synthesis of 3- or 5-silylpyrazoles and...
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Published in | Tetrahedron Vol. 62; no. 4; pp. 611 - 618 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
OXFORD
Elsevier Ltd
23.01.2006
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Silyl β-enaminones have been synthesized by reductive cleavage of 5-silyl, 3-, 4- and 5-silylmethylisoxazoles.These versatile synthons bearing different silyl groups in various positions of the enaminoketonic system are of great interest in the regioselective synthesis of 3- or 5-silylpyrazoles and 3-, 4- or 5-silylmethylpyrazoles, which can serve as building blocks in heterocyclic chemistry.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2005.10.001 |