@article{oai:kanazawa-u.repo.nii.ac.jp:00014870,
 author = {Matsuo, Jun-ichi and Tanaki, Yumi and Ishibashi, Hiroyuki},
 issue = {22},
 journal = {Tetrahedron},
 month = {May},
 note = {Indolenines were generated at -78 °C from 3-benzylic or 3-allylic indoles by dehydrogenation with N-tert-butylbenzenesulfinimidoyl chloride, and a carbon-carbon bond was formed at -78 °C in a one-pot manner by treating these indolenines with various carbon nucleophiles such as active methylene compounds or organocuprates. © 2008 Elsevier Ltd. All rights reserved., 金沢大学医薬保健研究域薬学系},
 pages = {5262--5267},
 title = {One-pot oxidative carbon-carbon bond formation of 3-benzylic and 3-allylic indoles with carbon nucleophiles},
 volume = {64},
 year = {2008}
}