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α,β-Unsaturated Fischer Carbene Complexes vs. 1,3-Dipoles: Reactions with Nitrones and Nitrilimines

✍ Scribed by José Barluenga; Félix Fernández-Marí; Rosario González; Enrique Aguilar; Gustavo A. Revelli; Argimiro L. Viado; Francisco J. Fañanás; Bernardo Olano


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
428 KB
Volume
2000
Category
Article
ISSN
1434-193X

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✦ Synopsis


The reaction of tert-butylalkynyl chromium Fischer carbene complex 1 with nitrones 2 affords β-enamino-ketoaldehydes 4 by the light-promoted rearrangement of the corresponding [3+2] cycloadduct carbene complexes 3. On the other hand,


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The chemistry of stabilized Group 6 metal carbene complexes (Fischer carbenes) has reached a high level of maturity and carbenes have become very valuable building blocks in organic synthesis. In spite of this, the reactivity of highly reduced Fischer carbene complexes has been somewhat neglected.