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Volumn 69, Issue 31, 2013, Pages 6507-6511

Enantiospecific formal total synthesis of (+)-aspicilin

Author keywords

Desymmetrization; Macrolactone; Olefin metathesis; Tartaric acid; Yamaguchi macrolactonization

Indexed keywords

ALKENE; AMIDE; ASPICILIN; MACROLIDE; TARTARIC ACID; UNCLASSIFIED DRUG;

EID: 84879240447     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.041     Document Type: Article
Times cited : (8)

References (39)
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    • 33846245038 scopus 로고    scopus 로고
    • For the synthesis of γ-hydroxy amides from tartaric acid, see
    • For the synthesis of γ-hydroxy amides from tartaric acid, see: K.R. Prasad, and A. Chandrakumar Tetrahedron 63 2007 1798
    • (2007) Tetrahedron , vol.63 , pp. 1798
    • Prasad, K.R.1    Chandrakumar, A.2
  • 35
    • 33845278635 scopus 로고
    • The dimethyl amide 5 was prepared from diethyl tartrate in a two-step sequence according to the procedure described in literature
    • The dimethyl amide 5 was prepared from diethyl tartrate in a two-step sequence according to the procedure described in literature F. Toda, and K. Tanaka J. Org. Chem. 53 1988 3607
    • (1988) J. Org. Chem. , vol.53 , pp. 3607
    • Toda, F.1    Tanaka, K.2
  • 36
    • 34547619995 scopus 로고    scopus 로고
    • 1H NMR Spectroscopy. Configuration of the major diastereomer was assigned analogous to the reduction of structurally similar ketones. See: No efforts were made to separate the minute amount of minor isomer
    • 1H NMR Spectroscopy. Configuration of the major diastereomer was assigned analogous to the reduction of structurally similar ketones. See: K.R. Prasad, and A. Chandrakumar J. Org. Chem. 72 2007 6312 No efforts were made to separate the minute amount of minor isomer
    • (2007) J. Org. Chem. , vol.72 , pp. 6312
    • Prasad, K.R.1    Chandrakumar, A.2
  • 38
    • 67649418184 scopus 로고    scopus 로고
    • (S)-7-Octen-2-ol has been prepared following a procedure similar to that described for the synthesis of (S)-6-hepten-2-ol. See
    • (S)-7-Octen-2-ol has been prepared following a procedure similar to that described for the synthesis of (S)-6-hepten-2-ol. See: M.-Y. Kim, H. Kim, and J. Tae Synlett 2009 1303
    • (2009) Synlett , pp. 1303
    • Kim, M.-Y.1    Kim, H.2    Tae, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.