@article{oai:kanazawa-u.repo.nii.ac.jp:00014941,
 author = {Yamada, Koji and Yamada, Fumio and Somei, Masanori},
 issue = {2},
 journal = {Heterocycles},
 month = {Mar},
 note = {1-Hydroxytryptamine derivatives undergo nucleophilic substitution reaction on the indole nitrogen (Na) as a general reaction by the treatment with acid, providing a novel synthetic method for 1-aryltryptamines. Depending on the structures of nucleophiles, 5- and 7-substituted tryptamines can also be produced in addition to the 1-aryltryptamines., An easy approach to 7-substituted 4,5-dihydro-7H-pyrano[3,4-c]-isoxazole derivatives (3a-b and 6a-d) is described by the reaction of 2-aryl substituted 1-nitro-3-oxa-6-heptynes (2, 5a and 5b) with n-BuLi, followed by treatment with acetic anhydride., 金沢大学大学院自然科学研究科生理活性物質科学},
 pages = {685--690},
 title = {Preparation of 7-substituted 4,5-dihydro-7H-pyrano[3,4-c]-isoxazole derivatives},
 volume = {59},
 year = {2002}
}