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Volumn 44, Issue 5, 1996, Pages 1138-1140

Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 9-alkylated benzolactams

Author keywords

benzolactam; hydrophobic interaction; structure activity relation; teleocidin; tumor promoter

Indexed keywords

BENZENE DERIVATIVE; INDOLACTAM V; LACTAM DERIVATIVE; TELEOCIDIN;

EID: 0029974959     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.44.1138     Document Type: Article
Times cited : (19)

References (22)
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    • Ohno M., Endo Y., Hirano M., Itai A., Shudo K., Tetrahedron Lett., 34, 8119-8122 (1993); Endo Y., Ohno M., Hirano M., Takeda M., Itai A., Shudo K., BioMed. Chem. Lett., 4, 491-494 (1994); Endo Y., Ohno M., Hirano M., Itai A., Shudo K., J. Am. Chem. Soc., 118, 1841-1855 (1996).
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    • note
    • The transformation of 6 to 7 by the method used for BL-V8-310 (HCl-AcOH, heat) or the method used for IL-V (KOHaq, heat then HClaq, heat) gave a complex mixture, probably due to the decomposition of the m-nitrobromobenzene residue
  • 15
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    • note
    • In the first attempt at synthesis, substitution of the N-methyl derivative of 8 with the triflate was very slow and the hydrolysis did not proceed effectively.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.