Planta Medica, Inhaltsverzeichnis Planta Med 2004; 70(5): 452-457DOI: 10.1055/s-2004-818975 Original Paper Natural Product Chemistry © Georg Thieme Verlag KG Stuttgart · New York Diterpenoids from Salvia wagneriana Angela Bisio1 , Nunziatina De Tommasi2 , Giovanni Romussi1 1Dipartimento di Chimica e Tecnologie Farmaceutiche e Alimentari, Università di Genova, Genova, Italy 2Dipartimento di Scienze Farmaceutiche, Università di Salerno, Salerno, Italy Artikel empfehlen Abstract Artikel einzeln kaufen Abstract From the surface exudate of the aerial parts of Salvia wagneriana, three new clerodane diterpenoids, the known hardwickiic acid and 1,10-didehydrosalviarin, were obtained. Two were bis-diterpenoids. Their structures were established by 1D- and 2D-NMR spectroscopic techniques. Key words Salvia wagneriana - Lamiaceae - clerodane diterpenes - bis-clerodane diterpenes - insecticidal - antifeedant Volltext Referenzen References 1 Penso G. Index plantarum medicinalium totius mundi eorumque synonymorum. Milano; OEMF 1983: pp 845-8 2 Zepernick B, Langhammer L, Lüdcke J BP. Lexikon der offizinellen Arzneipflanzen. Berlin; Walter de Gruyter 1984: pp 366-9 3 Rodríguez Hahn L, Esquivel B, Cárdenas J, Ramamoorthy T P. The Distribution of Diterpenoids in Salvia . In: Harley RM and Reynolds, editors Advances in Labiatae Science. Kew; Royal Botanic Gardens 1992: pp 335-45 4 Romussi G, Ciarallo G, Bisio A, Fontana N, De Simone F, De Tommasi N, Mascolo N, Pinto L. A new diterpenoid with antispasmodic activity from Salvia cinnabarina . Planta Medica. 2001; 67 153-5 5 Epling C. A Revision of Salvia, subgenus Calosphace. In: Fedde F, editor Repertorium Specierum Novarum Regni Vegetabilis. Vol. CX Berlin: Dahlem; 1939: p 139 6 Bandara Ratnayake B M, Wimalasiri W R, Bandara Premaratne K AN. Isolation and insecticidal activity of (-)-hardwickiic acid from Croton aromaticus . Planta Medica. 1987; 53 575 7 Simmonds M SJ, Blaney W M, Esquivel B, Rodríguez Hahn L. Effect of clerodane-type diterpenoids isolated from Salvia spp. on the feeding behaviour of Spodoptera littoralis . Pesticide Science. 1996; 47 17-23 8 McChesney J D, Silveira E R. 12-Hydroxyhardwickic acid and sonderanial, neo-clerodanes from Croton sonderianus . Phytochemistry. 1989; 28 3411-4 9 Zdero C, Bohlmann F, King R M. Diterpenes and norditerpenes from the Aristeguetia group. Phytochemistry. 1991; 30 2991-3000 10 Misra R, Pandey R C, Dev S. Diterpenoids from the oleoresin of Hardwickia pinnata part 1: hardwickiic acid. Tetrahedron. 1979; 35 2301-10 11 Briesekorn C H, Stehle T. Bitter principles of Labiatae: A new compound of the clerodane type. Chemische Berichte. 1973; 106 922-8 12 Esquivel B, Cárdenas J, Ramamoorthy T P, Rodríguez Hahn L. Clerodane diterpenoids of Salvia lineata . Phytochemistry. 1986; 25 2381-4 13 Rodríguez-Hahn L, Esquivel B, Cárdenas J. Clerodane Diterpenes in Labiatae. In: Zechmeister L, editor Progress in the Chemistry of Organic Natural Products. Vol. LXIII Heidelberg; Springer 1994: p 141 Prof. Dr. G. Romussi Dipartimento di Chimica e Tecnologie Farmaceutiche e Alimentari Via Brigata Salerno 16147 Genova Italy Fax: +39-010-353-2684 eMail: romussi@dictfa.unige.it