{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,13]],"date-time":"2025-10-13T19:48:45Z","timestamp":1760384925485},"reference-count":10,"publisher":"CLOCKSS Archive","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["HETEROCYCLES"],"published-print":{"date-parts":[[2002]]},"DOI":"10.3987\/com-02-9503","type":"journal-article","created":{"date-parts":[[2009,3,9]],"date-time":"2009-03-09T01:54:48Z","timestamp":1236563688000},"page":"1231","source":"Crossref","is-referenced-by-count":9,"title":["Reactions of 1-Methoxy-3-(2-nitrovinyl)- indole with Nucleophiles: An Interesting Solvent Effect and a Novel Preparation of 3-Substituted 1-Methoxyindoles"],"prefix":"10.13030","volume":"57","author":[{"given":"Masanori","family":"Somei","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Koji","family":"Yamada","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fumio","family":"Yamada","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"5187","reference":[{"key":"#cr-split#-10.3987\/COM-02-9503-1.1","unstructured":"a) This report is Part 114 of a series entitled \u201cThe Chemistry of Indoles\u201d and partly reported at the 120th Annual Meeting of Pharmaceutical Society of Japan, Book of Abstracts 2, Gifu, March 2000, p. 32."},{"key":"#cr-split#-10.3987\/COM-02-9503-1.2","unstructured":"1. a) This report is Part 114 of a series entitled \u201cThe Chemistry of Indoles\u201d and partly reported at the 120th Annual Meeting of Pharmaceutical Society of Japan, Book of Abstracts 2, Gifu, March 2000, p. 32. b) Part 113: K. Yamada, F. Yamada, T. Shiraishi, S. Tomioka, and M. Somei, Heterocycles, 58 (2002), in press. c) All new compounds gave satisfactory spectral and elemental analysis or high-resolution MS data for crystals or oils, respectively. 4a) mp 209—212\u00b0C (decomp); 4b) mp 191—198\u00b0C (decomp); 4c) mp 124—129\u00b0C (decomp); 6a) mp 101—102\u00b0C; 6b) yellow viscous oil; 6c) yellow viscous oil; 6d) mp 85—86\u00b0C; 7) yellow viscous oil; 8a) mp 218—219\u00b0C (decomp); 8b) mp 217—222\u00b0C (decomp); 8c) mp 176.5—177.0\u00b0C; 9) yellow viscous oil; 10) mp 91.0—91.5\u00b0C; 11) yellow viscous oil; 12) yellow viscous oil."},{"key":"#cr-split#-10.3987\/COM-02-9503-1.3","unstructured":"c) All new compounds gave satisfactory spectral and elemental analysis or high-resolution MS data for crystals or oils, respectively. 4a) mp 209-212\u00b0C (decomp); 4b) mp 191-198\u00b0C (decomp); 4c) mp 124-129\u00b0C (decomp); 6a) mp 101-102\u00b0C; 6b) yellow viscous oil; 6c) yellow viscous oil; 6d) mp 85-86\u00b0C; 7) yellow viscous oil; 8a) mp 218-219\u00b0C (decomp); 8b) mp 217-222\u00b0C (decomp); 8c) mp 176.5-177.0\u00b0C; 9) yellow viscous oil; 10) mp 91.0-91.5\u00b0C; 11) yellow viscous oil; 12) yellow viscous oil."},{"key":"10.3987\/COM-02-9503-2","doi-asserted-by":"crossref","unstructured":"2. Review: M. Somei, Heterocycles, 1999, 50, 1157; M. Somei, N. Oshikiri, M. Hasegawa, and F. Yamada, ibid., 1999, 51, 1237; M. Somei, M. Nakajou, T. Teramoto, and F. Yamada, ibid., 1999, 51, 1949; M. Hasegawa, K. Yamada, Y. Nagahama, and M. Somei, ibid., 1999, 51, 2815; T. Kurauchi, Y. Nagahama, M. Hasegawa, K. Yamada, and M. Somei, ibid., 2000, 53, 1017; F. Yamada, A. Goto, and M. Somei, ibid., 2000, 53, 1255; M. Somei, Y. Fukui, M. Hasegawa, N. Oshikiri, and T. Hayashi, ibid., 2000, 53, 1725; M. Somei, F. Yamada, T. Kurauchi, Y. Nagahama, M. Hasegawa, K. Yamada, S. Teranishi, H. Sato, and C. Kaneko, Chem. Pharm. Bull., 2001, 49, 87; M. Somei, F. Yamada, T. Hayashi, A. Goto, and Y. Saga, Heterocycles, 2001, 55, 457; K. Yamada, T. Kawasaki, Y. Fujita, and M. Somei, ibid., 2001, 55, 1151; T. Hayashi, W. Peng, Y. Nakai, K. Yamada, and M. Somei, ibid., 2002, 56, 421.","DOI":"10.3987\/REV-98-SR(H)8"},{"key":"10.3987\/COM-02-9503-3","unstructured":"3. R. J. Sundberg, \u201cThe Chemistry of Indoles,\u201d Academic Press, New York, 1970; R. J. Sundberg, \u201cIndoles,\u201d Academic Press, New York, 1996."},{"key":"#cr-split#-10.3987\/COM-02-9503-4.1","doi-asserted-by":"crossref","unstructured":"a) M. Somei, F. Yamada, T. Izumi, and M. Nakajou, Heterocycles, 1997, 45, 2327;","DOI":"10.3987\/COM-97-7989"},{"key":"#cr-split#-10.3987\/COM-02-9503-4.2","doi-asserted-by":"crossref","unstructured":"b) M. Somei, A. Tanimoto, H. Orita, F. Yamada, and T. Ohta, ibid., 2001, 54, 425. See also reference 1b.","DOI":"10.3987\/COM-00-S(I)12"},{"key":"10.3987\/COM-02-9503-5","unstructured":"5. C. Reichardt, \u201cSolvent Effects in Organic Chemistry,\u201d 3, Verlag Chemie GmbH, Weinheim, 1979."},{"key":"10.3987\/COM-02-9503-6","doi-asserted-by":"crossref","unstructured":"6. Related cycloadditions of nitronates: S. E. Denmark and A. Thorarensen, Chem. Rev., 1996, 96, 137; G. Broggini and G. Zecchi, Synthesis, 1999, 905 and references cited therein.","DOI":"10.1021\/cr940277f"},{"key":"10.3987\/COM-02-9503-7","doi-asserted-by":"crossref","unstructured":"7. A. Hassner, O. Friedman, and W. Dehaen, Liebigs Ann., 1997, 587.","DOI":"10.1002\/jlac.199719970321"}],"container-title":["HETEROCYCLES"],"original-title":[],"language":"en","deposited":{"date-parts":[[2024,6,24]],"date-time":"2024-06-24T20:34:20Z","timestamp":1719261260000},"score":1,"resource":{"primary":{"URL":"https:\/\/triggered.stanford.clockss.org\/ServeContent?doi=10.3987%2Fcom-02-9503"},"secondary":[{"URL":"https:\/\/triggered.edinburgh.clockss.org\/ServeContent?doi=10.3987%2Fcom-02-9503","label":"edinburgh"}]},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2002]]},"references-count":10,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2002]]}},"alternative-id":["COM-02-9503"],"URL":"https:\/\/doi.org\/10.3987\/com-02-9503","relation":{},"ISSN":["0385-5414"],"issn-type":[{"type":"print","value":"0385-5414"}],"subject":[],"published":{"date-parts":[[2002]]}}}