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Volumn 43, Issue 44, 2002, Pages 7933-7936

Synthesis of oxygenated spongiane-type diterpenoids from carvone

Author keywords

[No Author keywords available]

Indexed keywords

CARVONE; DITERPENOID; FURAN DERIVATIVE;

EID: 0037190881     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01891-9     Document Type: Article
Times cited : (9)

References (25)
  • 2
    • 0036007872 scopus 로고    scopus 로고
    • and previous reviews of this series
    • Faulkner D.J. Nat. Prod. Rep. 19:2002;1-48. and previous reviews of this series.
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 1-48
    • Faulkner, D.J.1
  • 18
    • 33748600689 scopus 로고    scopus 로고
    • Ref. 1
    • For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
  • 19
    • 33748600689 scopus 로고    scopus 로고
    • For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
    • (1998) J. Chem. Soc., Perkin Trans. 1 , pp. 863-868
    • Pattenden, G.1    Roberts, L.2    Blake, A.J.3
  • 20
    • 0034957110 scopus 로고    scopus 로고
    • and references cited therein
    • For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
    • (2001) Synthesis , pp. 1114-1116
    • Goeller, F.1    Heinemann, C.2    Demuth, M.3
  • 22
    • 0010691569 scopus 로고    scopus 로고
    • The stereochemistry of the Diels-Alder adduct formed was assigned on the basis of intramolecular NOE studies. In particular, no NOE was observed upon irradiation of either the Me-8 (δ 1.25 ppm) or the Me-10 (δ 0.98 ppm) on each other, which strongly suggested the anti disposition of both methyl groups.
    • The stereochemistry of the Diels-Alder adduct formed was assigned on the basis of intramolecular NOE studies. In particular, no NOE was observed upon irradiation of either the Me-8 (δ 1.25 ppm) or the Me-10 (δ 0.98 ppm) on each other, which strongly suggested the anti disposition of both methyl groups.
  • 24
    • 0010734680 scopus 로고    scopus 로고
    • -3.
    • -3.
  • 25
    • 0010693224 scopus 로고    scopus 로고
    • note
    • 4′).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.