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Volumn 74, Issue 19, 2009, Pages 7457-7463

Enantioselective synthesis of the R-enantiomer of the feeding deterrent (S)-ypaoamide

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; ENANTIOMERS;

EID: 70349456661     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901557h     Document Type: Article
Times cited : (43)

References (54)
  • 1
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    • The Discovery of Marine Natural Products with Therapeutic Potential
    • For reviews, see: (a) Gullo, V., Ed.: Springer-Verlag: New York
    • For reviews, see: (a) McConnell, O. J.; Longley, R. E.; Koehn, F. E. The Discovery of Marine Natural Products with Therapeutic Potential. In The Discovery of Natural Products with Therapeutic Potential: Gullo, V., Ed.: Springer-Verlag: New York, 1994; pp 109-174.
    • (1994) The Discovery of Natural Products with Therapeutic Potential , pp. 109-174
    • McConnell, O.J.1    Longley, R.E.2    Koehn, F.E.3
  • 16
    • 0029941610 scopus 로고    scopus 로고
    • For the total synthesis of microcolin A, see: (a)
    • For the total synthesis of microcolin A, see: (a) Decicco, C. P.; Grover, P. J. Org. Chem. 1996, 61, 3534-3541.
    • (1996) J. Org. Chem. , vol.61 , pp. 3534-3541
    • Decicco, C.P.1    Grover, P.2
  • 17
    • 0001271376 scopus 로고    scopus 로고
    • For the total synthesis of microcolin B, see: (b)
    • For the total synthesis of microcolin B, see: (b) Andrus, M. B.; Li, W.-K.; Keyes, R. E. J. Org. Chem. 1997, 62, 5542-5549.
    • (1997) J. Org. Chem. , vol.62 , pp. 5542-5549
    • Andrus, M.B.1    Li, W.-K.2    Keyes, R.E.3
  • 18
    • 0030041206 scopus 로고    scopus 로고
    • For synthetic studies on microcolin B, see: (c)
    • For synthetic studies on microcolin B, see: (c) Mattern, R. H.; Gunasekera, S.; McConnell, O. Tetrahedron 1996, 52, 425-434.
    • (1996) Tetrahedron , vol.52 , pp. 425-434
    • Mattern, R.H.1    Gunasekera, S.2    McConnell, O.3
  • 25
    • 0027399591 scopus 로고
    • For amino acid-based synthetic approaches to 5-alkyl-3-pyrrolin-2- ones, see: (a)
    • For amino acid-based synthetic approaches to 5-alkyl-3-pyrrolin-2- ones, see: (a) Schmidt, U.; Riedl, B.; Haas, G.; Griesser, H.; Vetter, A.; Weinbrenner, S. Synthesis 1993, 216-220.
    • (1993) Synthesis , pp. 216-220
    • Schmidt, U.1    Riedl, B.2    Haas, G.3    Griesser, H.4    Vetter, A.5    Weinbrenner, S.6
  • 31
    • 0032557508 scopus 로고    scopus 로고
    • For nonamino acid-based synthetic approaches to 5-alkyl-3-pyrrolin- 2-ones, see: (a)
    • For nonamino acid-based synthetic approaches to 5-alkyl-3-pyrrolin- 2-ones, see: (a) Merino, P.; Castillo, E.; Franco, S.; Merchan, F. L.; Tejero, T. Tetrahedron: Asymmetry 1998, 9, 1759-1769.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 1759-1769
    • Merino, P.1    Castillo, E.2    Franco, S.3    Merchan, F.L.4    Tejero, T.5
  • 53
    • 33846209146 scopus 로고    scopus 로고
    • For a review on the enzymatic catalyzed reaction, see
    • For a review on the enzymatic catalyzed reaction, see: Ghanem, A. Tetrahedron 2007, 63, 1721-1754.
    • (2007) Tetrahedron , vol.63 , pp. 1721-1754
    • Ghanem, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.