Synthesis and reactions of the first cyclopentadienyl isonitriles
✍ Scribed by Klaus Banert; Frank Köhler; Barbara Meier
- Book ID
- 104253554
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 109 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Azidofulvenes without a further substituent in the exocyclic position were transformed into new 1-isocyano-and 2-isocyanocyclopenta-1,3-dienes by photolysis in methanol. These novel functionalized cyclopentadienes are useful building blocks, e.g. as dienes in Diels-Alder reactions.
📜 SIMILAR VOLUMES
Isonitriles react with carbenes to give @-adducts, keteneimines. 1) Further cycloaddition of isonitriles to keteneimines is expected when the substituents of them are aromatic. From this point of view, reaction of several aromatic isonitriles with diazoalkanes as the precursors of carbene was examin
## Abstract Cyclopentadienyl–ruthenium half‐sandwich complexes with η^2^‐bound alkyne ligands have been suggested as catalytic intermediates in the early stages of Ru‐catalyzed reactions with alkynes. We show that electronically unsaturated complexes of the formula [RuCl(Cp^)(η^2^‐RC≡CR′)] can be s
Acetyl and benzyl protected 13-D-glucopyranosyl isonitriles were treated with various aldehydes and acetic acid to give the corresponding Passerini reaction products and with i-butanal, carboxylic acids and amines to give the corresponding Ugi reaction products, respectively. No significant diastere