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,
📜 SIMILAR VOLUMES
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.