Selective Alkene Insertion into Inert Hydrogen–Metal Bonds Catalyzed by Mono(phosphorus ligand)palladium(0) Complexes
Author:
Affiliation:
1. Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16, Nakacho, Koganei, Tokyo 184-8588, Japan
Funder
Japan Society for the Promotion of Science
Tokyo University of Agriculture
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.7b00593
Reference43 articles.
1. aComprehensive Organic Synthesis;Trost, B. M. and Fleming, I., Eds.Elsevier:Oxford, U.K., 1991; Vol.8, pp667–792.
2. 116. Chemistry of the metal carbonyls. Part XXI. New complexes derived from manganese pentacarbonyl hydride, π-cyclopentadienyl-molybdenum tricarbonyl hydride, and π-cyclopentadienyltungsten tricarbonyl hydride
3. Transition-metal-cyanocarbon chemistry. 2. Cyanoacetylenes insertions into the metal-hydrogen bond of (.eta.5-C5H5)(CO)3MH (M = Mo, W) complexes. Formation of phosphorus ylide complexes and the structure of (.eta.5-C5H5)(CO)2Mo[.eta.2-C(CN)PPh3CHCN]
4. Acid-Catalyzed Carbonylation of Lactone to Cyclic Anhydride on Tungsten Metal
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