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Volumn 76, Issue 7, 2011, Pages 2132-2144

Solid phase synthesis of globomycin and SF-1902 A5

Author keywords

[No Author keywords available]

Indexed keywords

GLOBOMYCIN; LIPIDIC CHAIN; MACROLACTONIZATION; PEPTIDIC FRAGMENTS; SIGNAL PEPTIDASE; SOLID PHASE SYNTHESIS; SOLID SUPPORTS; SOLID-PHASE;

EID: 79953186077     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1025145     Document Type: Article
Times cited : (29)

References (91)
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    • The synthesis of this amino acid derivative is described in Supporting Information.
    • The synthesis of this amino acid derivative is described in Supporting Information.
  • 69
    • 79953200070 scopus 로고    scopus 로고
    • See Supporting Information for the description of hydroxyl silylethers SI-2 and SI-3.
    • See Supporting Information for the description of hydroxyl silylethers SI-2 and SI-3.
  • 73
    • 60849094459 scopus 로고    scopus 로고
    • Preparation of epoxy alcohol 30 and its enantiomer by Sharpless asymmetric epoxidation were reported by Kitching; (24) however yields were not reported. Later, the enantiomer of 30 was described in 95% yield
    • Preparation of epoxy alcohol 30 and its enantiomer by Sharpless asymmetric epoxidation were reported by Kitching; (24) however yields were not reported. Later, the enantiomer of 30 was described in 95% yield: Ortega, N.; Martín, T.; Martín, V. S. Eur. J. Org. Chem. 2009, 554-563
    • (2009) Eur. J. Org. Chem. , pp. 554-563
    • Ortega, N.1    Martín, T.2    Martín, V.S.3
  • 75
    • 20444432673 scopus 로고    scopus 로고
    • As for 30, the synthesis of the enantiomer of epoxy alcohol 31 via Sharpless asymmetric epoxidation in 52% yield has been reported
    • As for 30, the synthesis of the enantiomer of epoxy alcohol 31 via Sharpless asymmetric epoxidation in 52% yield has been reported: Tanaka, T.; Hiramatsu, K.; Kobayashi, Y.; Ohno, H. Tetrahedron 2005, 61, 6726-6742
    • (2005) Tetrahedron , vol.61 , pp. 6726-6742
    • Tanaka, T.1    Hiramatsu, K.2    Kobayashi, Y.3    Ohno, H.4
  • 80
    • 33645950428 scopus 로고    scopus 로고
    • Recent examples of amides hydrolysis under acidic conditions
    • Recent examples of amides hydrolysis under acidic conditions: Arpin, A.; Manthorpe, J. M.; Gleason, J. L. Org. Lett. 2006, 8, 1359-1362
    • (2006) Org. Lett. , vol.8 , pp. 1359-1362
    • Arpin, A.1    Manthorpe, J.M.2    Gleason, J.L.3
  • 85
    • 70349894955 scopus 로고    scopus 로고
    • For recent examples of N -Boc activation of amides, see
    • For recent examples of N -Boc activation of amides, see: Liu, W.-J.; Lv, B.-D.; Gong, L.-Z. Angew. Chem., Int. Ed. 2009, 48, 6503-6506
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6503-6506
    • Liu, W.-J.1    Lv, B.-D.2    Gong, L.-Z.3
  • 87
    • 77954644732 scopus 로고    scopus 로고
    • For a recent example of N -sulfonyl activation of amides, see
    • For a recent example of N -sulfonyl activation of amides, see: Liau, B. B.; Shair, M. D. J. Am. Chem. Soc. 2010, 132, 9594-9595
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 9594-9595
    • Liau, B.B.1    Shair, M.D.2
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    • See the Supporting Information for general techniques.
    • See the Supporting Information for general techniques.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.