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Volumn 63, Issue 8, 2007, Pages 1798-1805

Stereoselective syntheses of γ-alkyl (aryl)-α,β-dihydroxy-γ-butyrolactones and naturally occurring lipid guggultetrol

Author keywords

Butyrolactone; Guggultetrol; l (+) Tartaric acid; Stereoselective reduction

Indexed keywords

AMIDE; GAMMA BUTYROLACTONE DERIVATIVE; GAMMA OXOBUTYRAMIDE; GUGGULSTERONE; GUGGULTETROL; TARTARIC ACID; UNCLASSIFIED DRUG;

EID: 33846245038     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.12.037     Document Type: Article
Times cited : (44)

References (35)
  • 8
    • 33846186171 scopus 로고    scopus 로고
    • For synthesis of γ-alkyl (aryl)-α,β-dihydroxy-γ-butyrolactones see:
  • 16
    • 33846206669 scopus 로고    scopus 로고
    • For the use of α,β-dihydroxy-γ-butyrolactones in the synthesis of bio-active natural products:
  • 24
    • 33846264743 scopus 로고    scopus 로고
    • note
    • Stereochemistry of the alcohols 3h-j was further confirmed by X-ray crystal structure of compound 3j (the crystallographic data have been deposited with The Cambridge Crystallographic Data Centre, CCDC 618908). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data request/cif.
  • 25
    • 33846226860 scopus 로고    scopus 로고
    • note
    • 3OD solution of the lactone 4i (NMR sample) showed gradual epimerization over the days and almost complete epimerization at the C2-centre after 40 days standing at room temperature.
  • 26
    • 33846229872 scopus 로고    scopus 로고
    • note
    • The crystallographic data have been deposited with The Cambridge Crystallographic Data Centre CCDC 618909. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/data request/cif.
  • 27
    • 8744278061 scopus 로고    scopus 로고
    • For a review on sphingolipid synthesis see:
    • For a review on sphingolipid synthesis see:. Howell A.R., So R.C., and Richardson S.K. Tetrahedron 60 (2004) 11327
    • (2004) Tetrahedron , vol.60 , pp. 11327
    • Howell, A.R.1    So, R.C.2    Richardson, S.K.3
  • 28
    • 33846233194 scopus 로고    scopus 로고
    • For stereoselective synthesis and application of tetrols see:
  • 31
    • 33846222613 scopus 로고    scopus 로고
    • Isolation and assignment of absolute stereochemistry of guggultetrols:
  • 35
    • 0042130513 scopus 로고    scopus 로고
    • For a review on guggul lipids see:
    • For a review on guggul lipids see:. Urizar N.L., and Moore D.D. Annu. Rev. Nutr. 23 (2003) 303
    • (2003) Annu. Rev. Nutr. , vol.23 , pp. 303
    • Urizar, N.L.1    Moore, D.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.