메뉴 건너뛰기




Volumn 72, Issue 3, 2009, Pages 340-344

Genepolide, a sesterpene γ-lactone with a novel carbon skeleton from mountain wormwood (Artemisia umbelliformis)

Author keywords

[No Author keywords available]

Indexed keywords

ABSINTHOL; ALKADIENE; GAMMA LACTONE DERIVATIVE; GENEPOLIDE; SESTERTERPENE; UNCLASSIFIED DRUG;

EID: 65349106768     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np800468m     Document Type: Article
Times cited : (27)

References (41)
  • 1
    • 65349149521 scopus 로고    scopus 로고
    • Appendino, G.; Taglialatela-Scafati, O. Drug-like Compounds from Food Plants and Spices In Dietary Supplements of Plant Origin; Maffei, M., Ed.; Taylor & Francis: London, 2003; pp 43-74.
    • Appendino, G.; Taglialatela-Scafati, O. Drug-like Compounds from Food Plants and Spices In Dietary Supplements of Plant Origin; Maffei, M., Ed.; Taylor & Francis: London, 2003; pp 43-74.
  • 4
    • 43249128900 scopus 로고    scopus 로고
    • Colomer, R.; Lupu, R.; Papadimitropoulou, A.; Vellón, L.; Vázquez- Martin, A.; Brunet, J.; Fernández-Gutiérrez, A.; Segura-Carretero, A.; Menéndez, J. A. Clin. Transl. Oncol. 2008, 10, 30-34.
    • Colomer, R.; Lupu, R.; Papadimitropoulou, A.; Vellón, L.; Vázquez- Martin, A.; Brunet, J.; Fernández-Gutiérrez, A.; Segura-Carretero, A.; Menéndez, J. A. Clin. Transl. Oncol. 2008, 10, 30-34.
  • 8
    • 0004220832 scopus 로고
    • Pharmaceutical Products Press: New York
    • Tyler, V. E. In Herbs of Choice; Pharmaceutical Products Press: New York, 1994; pp 42-46.
    • (1994) Herbs of Choice , pp. 42-46
    • Tyler, V.E.1
  • 24
    • 65349123656 scopus 로고    scopus 로고
    • http://www.genepy.it.
  • 29
    • 0033237606 scopus 로고    scopus 로고
    • Myrcene reacts as a dienophile only under harsh thermal and acidic conditions (Yin, D.; Yin, D.; Fu, Z.; Li, Q. J. Mol. Catal. A: Chem 1999, 148, 87-95.) as testified by the lack of self-dimerization during its industrial production from the thermal (>400 °C) cracking of β-pinene. Dienophilic behavior has also been reported for its conjugated terminal double bond Matusch, R.; Haberlein, H. Liebigs Ann. Chem. 1987, 455-457.
    • Myrcene reacts as a dienophile only under harsh thermal and acidic conditions (Yin, D.; Yin, D.; Fu, Z.; Li, Q. J. Mol. Catal. A: Chem 1999, 148, 87-95.) as testified by the lack of self-dimerization during its industrial production from the thermal (>400 °C) cracking of β-pinene. Dienophilic behavior has also been reported for its conjugated terminal double bond (Matusch, R.; Haberlein, H. Liebigs Ann. Chem. 1987, 455-457.
  • 30
    • 65349121924 scopus 로고    scopus 로고
    • Actually, the thermal cycloreversion of exomethylene-γ-lactone Diels- Alder adducts during GC analysis was observed: J. Sporle, J.; Becker, H.; Gupta, M. P.; Veith, M.; Huch, V. Tetrahedron 1989, 45, 5003-5014. Spörle, J.; Becker, H.; Allen, N. S.; Gupta, M. P. Phytochemistry 1991, 30, 3043-3047.
    • Actually, the thermal cycloreversion of exomethylene-γ-lactone Diels- Alder adducts during GC analysis was observed: J. Sporle, J.; Becker, H.; Gupta, M. P.; Veith, M.; Huch, V. Tetrahedron 1989, 45, 5003-5014. Spörle, J.; Becker, H.; Allen, N. S.; Gupta, M. P. Phytochemistry 1991, 30, 3043-3047.
  • 38
    • 0030889255 scopus 로고    scopus 로고
    • The acid-catalyzed cyclization of medium-sized polyolefins is notoriously capricious in terms of reproducibility: Appendino, G, Jakupovic, J, Cravotto, G, Biavatti-Weber, M. Tetrahedron 1997, 53, 4681-4692. We found that the photochemical generation of HCl from the irradiation of chloroform gave very reproducible reactions see Experimental Section
    • The acid-catalyzed cyclization of medium-sized polyolefins is notoriously capricious in terms of reproducibility: Appendino, G.; Jakupovic, J.; Cravotto, G.; Biavatti-Weber, M. Tetrahedron 1997, 53, 4681-4692. We found that the photochemical generation of HCl from the irradiation of chloroform gave very reproducible reactions (see Experimental Section).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.