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Volumn 5, Issue 5, 2003, Pages 765-768

Synthesis of (±)-phloeodictine A1

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC ANTIBIOTIC; BROMINE DERIVATIVE; PHLOEODICTINE A1; UNCLASSIFIED DRUG; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; PYRIDINIUM DERIVATIVE; PYRROLE DERIVATIVE;

EID: 0037529211     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034042e     Document Type: Article
Times cited : (60)

References (25)
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    • note
    • 3PO.
  • 9
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    • For related compounds, see: (a) Jokić, M.; Škarić, V. J. Chem. Soc., Perkin Trans. 1 1989, 757-763. (b) Spiessens, L. I.; Anteunis, M. J. O. Bull. Soc. Chim. Belg. 1984, 93, 191-203.
    • (1989) J. Chem. Soc., Perkin Trans. 1 , pp. 757-763
    • Jokić, M.1    Škarić, V.2
  • 10
    • 0001146638 scopus 로고
    • For related compounds, see: (a) Jokić, M.; Škarić, V. J. Chem. Soc., Perkin Trans. 1 1989, 757-763. (b) Spiessens, L. I.; Anteunis, M. J. O. Bull. Soc. Chim. Belg. 1984, 93, 191-203.
    • (1984) Bull. Soc. Chim. Belg. , vol.93 , pp. 191-203
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  • 13
    • 0034226973 scopus 로고    scopus 로고
    • Unsaturated Grignard reagents were prepared in THF from Mg and the known ω-bromo-1-alkenes: Watson, M. D.; Wagener, K. B. Macromolecules 2000, 33, 5411-5417.
    • (2000) Macromolecules , vol.33 , pp. 5411-5417
    • Watson, M.D.1    Wagener, K.B.2
  • 14
    • 0141439671 scopus 로고    scopus 로고
    • note
    • N2 reaction with the chlorobutyl side chain.
  • 17
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    • PCT Int. Appl. Patent WO 9,514,027, 1995
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    • Slassi, A.1    Sumanas, R.2
  • 22
    • 0000650727 scopus 로고    scopus 로고
    • For similar cyclizations, see: (a) Ueda, T.; Oh, R.; Nagai, S.-i.; Sakakibara, J. J. Heterocycl. Chem. 1998, 35, 135-139. (b) Meszá rosová, K.; Holý, A.; Masojídková, M. Collect. Czech. Chem. Commun. 2000, 65, 1109-1125. (c) Le Merrer, Y.; Gauzy, L.; Gravier-Pelletier, C.; Depezay, J.-C. Bioorg. Med. Chem. 2000, 8, 307-320.
    • (1998) J. Heterocycl. Chem. , vol.35 , pp. 135-139
    • Ueda, T.1    Oh, R.2    Nagai, S.-I.3    Sakakibara, J.4
  • 23
    • 0034340253 scopus 로고    scopus 로고
    • For similar cyclizations, see: (a) Ueda, T.; Oh, R.; Nagai, S.-i.; Sakakibara, J. J. Heterocycl. Chem. 1998, 35, 135-139. (b) Meszá rosová, K.; Holý, A.; Masojídková, M. Collect. Czech. Chem. Commun. 2000, 65, 1109-1125. (c) Le Merrer, Y.; Gauzy, L.; Gravier-Pelletier, C.; Depezay, J.-C. Bioorg. Med. Chem. 2000, 8, 307-320.
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  • 24
    • 0033621928 scopus 로고    scopus 로고
    • For similar cyclizations, see: (a) Ueda, T.; Oh, R.; Nagai, S.-i.; Sakakibara, J. J. Heterocycl. Chem. 1998, 35, 135-139. (b) Meszá rosová, K.; Holý, A.; Masojídková, M. Collect. Czech. Chem. Commun. 2000, 65, 1109-1125. (c) Le Merrer, Y.; Gauzy, L.; Gravier-Pelletier, C.; Depezay, J.-C. Bioorg. Med. Chem. 2000, 8, 307-320.
    • (2000) Bioorg. Med. Chem. , vol.8 , pp. 307-320
    • Le Merrer, Y.1    Gauzy, L.2    Gravier-Pelletier, C.3    Depezay, J.-C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.