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Volumn 76, Issue 7, 2011, Pages 2029-2039

Enantioselective synthesis of possible diastereomers of heptadeca-1-ene-4,6-diyne-3,8,9,10-tetrol; Putative structure of a conjugated diyne natural product isolated from hydrocotyle leucocephala

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOMERS; ENANTIOSELECTIVE SYNTHESIS; NATURAL PRODUCTS; SPECTRAL DATA;

EID: 79953218030     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102201k     Document Type: Article
Times cited : (22)

References (25)
  • 6
    • 33846245038 scopus 로고    scopus 로고
    • For a general approach to the synthesis of γ-keto amides from tartaric acid, see:;, For recent application of γ-keto amides derived from tartaric acid in natural product synthesis see:; Synlett 2010, 1093
    • For a general approach to the synthesis of γ-keto amides from tartaric acid, see: Prasad, K. R.; Chandrakumar, A. Tetrahedron 2007, 63, 1798 For recent application of γ-keto amides derived from tartaric acid in natural product synthesis see: Prasad, K. R.; Pawar, A. B. Synlett 2010, 1093
    • (2007) Tetrahedron , vol.63 , pp. 1798
    • Prasad, K.R.1    Chandrakumar, A.2    Prasad, K.R.3    Pawar, A.B.4
  • 15
    • 79953212891 scopus 로고    scopus 로고
    • Minor diastereomer obtained in the reaction is separable at this stage by column chromatography.
    • Minor diastereomer obtained in the reaction is separable at this stage by column chromatography.
  • 19
    • 0041649970 scopus 로고
    • Preparative acetylenic chemistry
    • In; Elsevier: Amsterdam.
    • Brandsma, L. Preparative acetylenic chemistry. In Studies in Organic Chemistry; Elsevier: Amsterdam, 1988.
    • (1988) Studies in Organic Chemistry
    • Brandsma, L.1
  • 21
    • 79953222891 scopus 로고    scopus 로고
    • In addition to the required diyne 16, a varying amount (15-19%) of the homo coupled product of the bromoalkyne is also formed.
    • In addition to the required diyne 16, a varying amount (15-19%) of the homo coupled product of the bromoalkyne is also formed.
  • 25
    • 79953194399 scopus 로고    scopus 로고
    • Stereochemistry of the double bond is of no consequence as it is saturated in the next step.
    • Stereochemistry of the double bond is of no consequence as it is saturated in the next step.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.