메뉴 건너뛰기




Volumn , Issue 10, 2008, Pages 1526-1528

Formal total synthesis of benzylpedamide: The right half of (+)-pederin

Author keywords

Pedamide; Pederin; Synthesis

Indexed keywords

BENZYLPEDAMIDE; IODINE; NATURAL PRODUCT; PEDERIN; PYRAN;

EID: 46449128747     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/S-2008-1077788     Document Type: Article
Times cited : (10)

References (51)
  • 5
    • 46449107873 scopus 로고
    • Chem. Abstr. 1954, 48, 57887.
    • (1954) Chem. Abstr , vol.48 , pp. 57887
  • 9
    • 0001406859 scopus 로고
    • For total synthesis of pederin compounds, see: a
    • For total synthesis of pederin compounds, see: (a) Hong, C. Y.; Kishi, Y. J. Org. Chem. 1990, 55, 4242.
    • (1990) J. Org. Chem , vol.55 , pp. 4242
    • Hong, C.Y.1    Kishi, Y.2
  • 26
    • 0022400671 scopus 로고
    • For total synthesis of pederin compounds, see: a
    • For total synthesis of pederin compounds, see: (a) Nakata, T.; Nagao, S.; Oishi, T. Tetrahedron Lett. 1985, 26, 6465.
    • (1985) Tetrahedron Lett , vol.26 , pp. 6465
    • Nakata, T.1    Nagao, S.2    Oishi, T.3
  • 28
    • 0001199461 scopus 로고    scopus 로고
    • For synthesis of the left halves, see
    • For synthesis of the left halves, see: Trotter, N. S.; Nakata, T. Org. Lett. 1999, 1, 957.
    • (1999) Org. Lett , vol.1 , pp. 957
    • Trotter, N.S.1    Nakata, T.2
  • 39
  • 41
    • 33846213674 scopus 로고    scopus 로고
    • For synthesis of the right halves, see
    • For synthesis of the right halves, see: Zhong, H. M.; Sohn, J. H.; Rawal, H. V. J. Org. Chem. 2007, 72, 386.
    • (2007) J. Org. Chem , vol.72 , pp. 386
    • Zhong, H.M.1    Sohn, J.H.2    Rawal, H.V.3
  • 45
    • 46449117863 scopus 로고    scopus 로고
    • Compound similar to 9 has been synthesized in different steps. See ref. 5e.
    • Compound similar to 9 has been synthesized in different steps. See ref. 5e.
  • 50
    • 46449087208 scopus 로고    scopus 로고
    • These attempts include oxidating 12 with MCPBA, or aerobic oxidation in the presence of Bu3SnH, and hydrolyzation with H2O either in strong polar solvents or in the presence of a base.
    • These attempts include oxidating 12 with MCPBA, or aerobic oxidation in the presence of Bu3SnH, and hydrolyzation with H2O either in strong polar solvents or in the presence of a base.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.