## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis of enol and vinyl esters catalyzed by an iridium complex
β Scribed by Hideto Nakagawa; Yoshio Okimoto; Satoshi Sakaguchi; Yasutaka Ishii
- Book ID
- 104252572
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 269 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Enol and vinyl esters were successfully synthesized by the use of an iridium complex as a catalyst. The reaction of carboxylic acid with terminal alkynes in the presence of catalytic amounts of [Ir(cod)Cl] 2 and Na 2 CO 3 gave the corresponding 1-alkenyl esters. The addition of carboxylic acids to alkynes principally took place in the Markovnikov fashion. In addition, by the use of an Ir complex combined with NaOAc various vinyl esters were prepared through the transvinylation between carboxylic acids and vinyl acetate.
π SIMILAR VOLUMES
Regioselective enol ester formation results frcm the addition of saturated and unsaturated carboxylic acids to phenylacetylene in the presence of RuC13, RuClj/2PRj 01 R~C~~(PMe~)(arene~ catalysts. Mononuclear ruthenium complexes, such as RuC13 or RuClz(PR3)(arene), have been shown recently to be mor
Ru-vinylidene complexes, Cl 2 Ru{ C C(H) t But}(PCy 3 )(L) (L=PCy 3 or N-heterocyclic carbenes) reveal themselves as a versatile catalyst for the atom transfer radical addition (ATRA) of polyhalogenated alkanes to olefins, such as methylmethacrylate, styrene and 1-octene. Furthermore, these systems
## Abstract For Abstract see ChemInform Abstract in Full Text.