@article{oai:kanazawa-u.repo.nii.ac.jp:00014923,
 author = {Yamada, Koji and Yamada, Fumio and Somei, Masanori},
 issue = {7},
 journal = {Heterocycles},
 month = {Jul},
 note = {Nucleophiles react with 1-methoxy-3-(2-nitrovinyl)indole (3) at the 2-position regioselectively in a dipolar aprotic solvent (DMF or HMPA), while in THF they undergo Michael addition to the β-carbon of nitrovinyl side chain. Depending on bases employed, the resultant Michael addition products (6d, 10, and 11) are found to undergo interesting cyclizations to give novel 3-substituted 1-methoxyindoles (7, 9, and 12)., 金沢大学大学院自然科学研究科生理活性物質科学},
 pages = {1231--1234},
 title = {Reactions of 1-methoxy-3-(2-nitrovinyl)indole with nucleophiles: An interesting solvent effect and a novel preparation of 3-substituted 1-methoxyindoles},
 volume = {57},
 year = {2002}
}