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Volumn , Issue 6, 2005, Pages 797-799

Synthesis and establishment of stereochemistry of the unusual polyoxazole-thiazole based cyclopeptide YM-216391 isolated from Streptomyces nobilis

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPEPTIDE; NATURAL PRODUCT; OXAZOLE DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; YM 216391;

EID: 14644401735     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b416530f     Document Type: Article
Times cited : (34)

References (16)
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    • A. J. Phillips, Y. Uto, P. Wipf, M. J. Reno and D. R. Williams, Org. Lett., 2000, 2, 1165-1168; G. Pattenden and T. Thompson, Tetrahedron Lett., 2002, 43, 2459-2461; D. C. Palmer, Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A, John Wiley & Sons, Inc. Hoboken, New Jersey, 2003.
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    • John Wiley & Sons, Inc. Hoboken, New Jersey
    • A. J. Phillips, Y. Uto, P. Wipf, M. J. Reno and D. R. Williams, Org. Lett., 2000, 2, 1165-1168; G. Pattenden and T. Thompson, Tetrahedron Lett., 2002, 43, 2459-2461; D. C. Palmer, Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A, John Wiley & Sons, Inc. Hoboken, New Jersey, 2003.
    • (2003) Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A
    • Palmer, D.C.1
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    • (1986) Tetrahedron , vol.42 , pp. 6555-6564
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  • 10
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    • O. E. Jensen and A. Senning, Tetrahedron, 1986, 42, 6555-6564; M. P. Cava and M. I. Levinson, Tetrahedron, 1985, 41, 5061-5087; G. Lajoie, F. Lépine, L. Maziak and B. Belleau, Tetrahedron Lett., 1983, 24, 3815-3818; K. Clausen, M. Thorsen and S.-O. Lawesson, Tetrahedron, 1981, 37, 3635-3639.
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    • O. E. Jensen and A. Senning, Tetrahedron, 1986, 42, 6555-6564; M. P. Cava and M. I. Levinson, Tetrahedron, 1985, 41, 5061-5087; G. Lajoie, F. Lépine, L. Maziak and B. Belleau, Tetrahedron Lett., 1983, 24, 3815-3818; K. Clausen, M. Thorsen and S.-O. Lawesson, Tetrahedron, 1981, 37, 3635-3639.
    • (1981) Tetrahedron , vol.37 , pp. 3635-3639
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    • T. Hu and J. S. Panek, J. Am. Chem. Soc., 2002, 124, 11368-11378; K. J. Hale, J. Cai and G. Williams, Synlett., 1998, 149-152.
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    • Hu, T.1    Panek, J.S.2
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    • 0003104705 scopus 로고    scopus 로고
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  • 15
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    • note
    • 6) 9.15 (1H, s), 9.05 (1H, s), 8.95 (1H, s), 8.71 (1H, s), 8.58 (1H, d, J = 8.4 Hz), 8.47 (2H, d, J = 7.1 Hz), 8.47-8.40 (1H, m), 7.98 (1H, d, J = 5.6 Hz), 7.62-7.49 (3H, m), 5.13 (1H, dd, J = 17.2 and 8.9 Hz), 4.68 (1H, dd, J = 8.4 and 5.5 Hz), 4.20-4.08 (2H, m), 2.18-2.07 (1H, m), 2.06-1.98 (1H, m), 1.68-1.53 (1H, m), 1.29-1.13 (1H, m) and 1.02-0.71 (12H, m) ppm.
  • 16
    • 14644398459 scopus 로고    scopus 로고
    • note
    • +] requires 719.2012.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.