@article{oai:kanazawa-u.repo.nii.ac.jp:00043297,
 author = {山田, 文夫 and 染井, 正徳 and Yamada, Fumio and Goto, Aya and Hasegawa, Masakazu and Kobayashi, Kensuke and Somei, Masanori},
 issue = {2},
 journal = {Heterocycles},
 month = {Dec},
 note = {Various nucleophiles, such as indole, 1,2,3-trimethoxybenzene, anisole, phenol, and pyrrole, reacted with 1-hydroxy-Nb-trifluoroacetyltryptamine under the presence of mesyl chloride to give novel series of (3a,8acis)- 1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indoles having a substituent at the 3aposition. Their structures and by-products were strictly determined. © 2017 The Japan Institute of Heterocyclic Chemistry., Embargo Period 12 months, 金沢大学医薬保健研究域薬学系},
 pages = {844--861},
 title = {Nucleophilic substitution reactions on indole nucleus: Formation of (3a,8a-cis)-1,2,3,3a,8,8a-hexahydropyrrolo-[2,3-b]indoles having a substituent at the 3a-position},
 volume = {95},
 year = {2017}
}