@article{oai:kanazawa-u.repo.nii.ac.jp:00015219,
 author = {Kawaguchi, Yasuaki and Yasuda, Shigeo and Mukai, Chisato},
 issue = {14},
 journal = {Journal of Organic Chemistry},
 month = {Jul},
 note = {Treatment of the benzylallene-internal alkynes with [RhCl(CO)2]2 effected a cycloisomerization via a Csp2-H bond activation to produce the tricyclo[9.4.0.03,8]pentadecapentaene skeleton. The reaction mechanism via formation of the rhodabicyclo[4.3.0] intermediates and σ-bond metathesis between the Csp2-H bond on the benzene ring and the Csp2-RhIII bond was proposed. In addition, a plausible alternative mechanism for the previously reported cycloisomerization of the benzylallene-terminal alkynes could also be proposed. © 2017 American Chemical Society., Embargo Period 12 months},
 pages = {7666--7674},
 title = {Mechanistic Investigation of RhI-Catalyzed Cycloisomerization of Benzylallene-Internal Alkynes via C-H Activation},
 volume = {82},
 year = {2017}
}