@article{oai:kanazawa-u.repo.nii.ac.jp:00011021,
 author = {藤波, 修平 and 宇梶, 裕 and 猪股, 勝彦 and Sakata, Ryo and Iwamoto, Ryoji and Fujinami, Shuhei and Ukaji, Yutaka and Inomata, Katsuhiko},
 issue = {2},
 journal = {Heterocycles},
 month = {Feb},
 note = {t-Butyl 3,4-dialkyl-1H-pyrrole-2-carboxylates were oxidized with ochloranil in the presence of MeOH to afford the corresponding 5-methoxypyrrolin-2-one derivatives. The resulting 5-methoxypyrrolin-2-one was reacted with various nucleophiles under acidic conditions to afford the functionalized pyrrolinone derivatives in good yields. © The Japan Institute of Heterocyclic Chemistry., 金沢大学理工研究域物質化学系},
 pages = {1157--1162},
 title = {Oxidation of pyrrole-2-carboxylates with o-chloranil and its synthetic application},
 volume = {82},
 year = {2010}
}