Journal
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES
Volume 87, Issue 5, Pages 230-241Publisher
JAPAN ACAD
DOI: 10.2183/pjab.87.230
Keywords
transition-metal catalyst; catalytic reaction; carbon hydrogen bond; activation; ruthenium complex; addition to olefin
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, japan
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The direct addition of C-H ortho bonds in various aromatic. compounds such as ketones. esters, imines. imidates, nitrites. and aldehydes to olefins and acetylenes can he achieved with the aid of transition metal catalysts. The ruthenium catalyzed reaction is usually highly efficient and useful as a general synthetic method. The coordination to the metal center by a heteroatom in a directing group such as carbonyl and imino groups in aromatic compounds is the key step in this process. Mechanistically, the reductive elimination to form a C-C bond is the rate-determining step. While the C-H bond cleavage step is not.
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