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Volumn 105, Issue 12, 2005, Pages 4441-4482

Recent progress of the synthetic studies of biologically active marine cyclic peptides and depsipeptides

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; BACTERIA; DEHYDRATION; MARINE BIOLOGY; MOLECULAR STRUCTURE; OXIDATION; SYNTHESIS (CHEMICAL);

EID: 30744433322     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr0406312     Document Type: Review
Times cited : (254)

References (263)
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    • Abbreviations used for amino acids and the designations of peptides follow the rules of the IUPAC-IUB Commission on Biochemical Nomenclature in J. Biol. Chem. 1985, 260, 14. Amino acid symbols denote the L-configuration unless stated otherwise. For other abbreviations, see section 10.
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    • Gerwick, W.H.1    Tan, L.T.2    Sitachitta, N.3
  • 17
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    • 0041475925 scopus 로고    scopus 로고
    • For a recent review on cyclization of peptides and depsipeptides, see
    • For a recent review on cyclization of peptides and depsipeptides, see: Davis, J. S. J. Pept. Sci. 2003, 9, 471.
    • (2003) J. Pept. Sci. , vol.9 , pp. 471
    • Davis, J.S.1
  • 28
    • 1342302805 scopus 로고    scopus 로고
    • For a recent review on peptide coupling reagents, see: and references therein
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    • (2004) Tetrahedron , vol.60 , pp. 2447
    • Han, S.-Y.1    Kim, Y.-A.2
  • 32
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    • CMD is produced for battery manufacture, and its reactivity is stronger than ordinary so-called active manganese dioxide, see
    • CMD is produced for battery manufacture, and its reactivity is stronger than ordinary so-called active manganese dioxide, see: Aoyama, T.; Sonoda, N.; Yamauchi, M.; Toriyama, K.; Anzai, M.; Ando, A.; Shioiri, T. Synlett 1998, 35.
    • (1998) Synlett , pp. 35
    • Aoyama, T.1    Sonoda, N.2    Yamauchi, M.3    Toriyama, K.4    Anzai, M.5    Ando, A.6    Shioiri, T.7
  • 95
    • 0002259309 scopus 로고
    • Atta-ur-Rahman, Ed., Elsevier: New York, (Stereoselective Synthesis (Part C))
    • (b) Shioiri, T.; Hamada, Y. Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed., Elsevier: New York, 1989; Vol. 4 (Stereoselective Synthesis (Part C)), p 83.
    • (1989) Studies in Natural Products Chemistry , vol.4 , pp. 83
    • Shioiri, T.1    Hamada, Y.2
  • 97
    • 0009790123 scopus 로고    scopus 로고
    • 2, see: Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart and references therein
    • 2, see: Aoyama, T.; Shioiri, T. Science of Synthesis; Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart, 2002; Vol. 4, p 569 and references therein.
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    • (2005) Tetrahedron , vol.61 , pp. 1257
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  • 141
    • 0032916413 scopus 로고    scopus 로고
    • For the synthesis of phakellistatin 2, see
    • (b) For the synthesis of phakellistatin 2, see: Pettit, G. R.; Rhodes, M. R.; Tan, R. J. Nat. Prod. 1999, 62, 409.
    • (1999) J. Nat. Prod. , vol.62 , pp. 409
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.