The Ni-Mediated Cyclocarbonylation of Allyl Halides and Alkynes Made Catalytic. Evidence Supporting the Involvement of Pseudoradical NiI Species in the Mechanism-Reference-Cited by-同舟云学术

The Ni-Mediated Cyclocarbonylation of Allyl Halides and Alkynes Made Catalytic. Evidence Supporting the Involvement of Pseudoradical NiI Species in the Mechanism

Published:2005-07-07 Issue:30 Volume:127 Page:10476-10477
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nadal M. Lluïsa¹,Bosch Julia¹,Vila Josep M.¹,Klein Günter¹,Ricart Susagna¹,Moretó Josep M.¹

Affiliation:

1. Laboratori de Catálisi Homogenea, Institut de Ciència de Materials de Barcelona, (CSIC) Campus de la UAB, 08193 Bellaterra, Spain

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0525713

Reference23 articles.

1. Efficient Photoinduced Electron Transfer in a Rigid U-Shaped Tetrad Bearing Terminal Porphyrin and Viologen Units

2. Interannular diastereoselectivity in the hydroboration of functionalized 1-cyclohexylcyclohexenes

3. Influence of functional substitution of allyl halides on their ni(co)4 promoted carbonylative cycloaddition with acetylenes

4. Ring-fused and spiro cyclopentenones by Ni(CO)4-promoted intermolecular carbonylative cycloaddition of acetylenes with 3-halo- and 1-(halomethyl)cycloalkenes

5. Change of the Reaction Pattern by Methodological Variations in a Multicomponent Assembly Promoted by Ni Complexes

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