@article{oai:kanazawa-u.repo.nii.ac.jp:00015221,
 author = {Yasuda, Shigeo and Yokosawa, Haruna and Mukai, Chisato},
 issue = {7},
 journal = {Chemical and Pharmaceutical Bulletin},
 month = {Jan},
 note = {Treatment of the allenylazetidine–alkynes with a catalytic amount of [RhCl(CO)dppp]2 (dppp: 1,3-bis(diphenylphosphino)propane) effected the intramolecular hetero-[6+2]-type ring-closing reaction via the C–C bond cleavage of the azetidine ring to produce azabicyclo[6.4.0]dodecatriene derivatives in good to excellent yields. The formation of the oxa analogue could also be achieved.},
 pages = {805--810},
 title = {Construction of Azabicyclo[6.4.0]dodecatrienes Based on Rhodium(I)-Catalyzed Intramolecular [6+2] Cycloaddition between Azetidine, Allene, and Alkynes},
 volume = {64},
 year = {2016}
}