@article{oai:kanazawa-u.repo.nii.ac.jp:00015328,
 author = {Matsuo, Junichi and Hoshikawa, Takaya and Sasaki, Shun and Ishibashi, Hiroyuki},
 issue = {4},
 journal = {Chemical and Pharmaceutical Bulletin},
 month = {Apr},
 note = {Trialkylamine-mediated intramolecular cyclization of pent-4-enoyl chlorides was studied. Substitution with a tertiary alkyl group at the 2-position gave cyclopent-2-en-1-ones, while substitution with an aromatic group gave enol esters, which were formed by O-acylation of initially formed 3-chlorocyclopentanones with ketenes., 金沢大学医薬保健研究域薬学系},
 pages = {591--592},
 title = {Trialkylamine-mediated intramolecular acylation of akenes with carboxylic acid chlorides},
 volume = {58},
 year = {2010}
}