A pregeijerene isomer from Juniperus erectopatens foliage

Phytochemistry

Volumn 63, Issue 1, 2003, Pages 105-108

  Cool, Laurence G ^a   Adams, Robert P ^b  

^a FOREST PRODUCTS LABORATORY   (United States)

^b BAYLOR UNIVERSITY   (United States)

Author keywords

Cupressaceae; Dimethylcyclodecatriene; Foliage; Juniperus erectoputens; Pregeijerene B; Sesquiterpene

Indexed keywords

1,7 DIMETHYLCYCLODECA 1,4,7 TRIENE; 8ALPHA ACETOXYHEDYCARYOL; GERMACRANE SESQUITERPENOID; JUNIPERUS ERECTOPATENS EXTRACT; PLANT EXTRACT; PREGEIJERENE B; PREGEIJERENE DERIVATIVE; SESQUITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CHEMICAL BINDING; DRUG IDENTIFICATION; GEOMETRY; HYDROGENATION; INFRARED RADIATION; ISOLATION PROCEDURE; ISOMER; JUNIPERUS; JUNIPERUS ERECTOPATENS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHYTOCHEMISTRY; SPECIES IDENTIFICATION;

CHROMATOGRAPHY, GAS; HYDROCARBONS, CYCLIC; HYDROGENATION; ISOMERISM; JUNIPERUS; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANT LEAVES;

CUPRESSACEAE; JUNIPERUS;

EID: 0037403856     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(02)00752-5     Document Type: Article

References (14)

1. Adams, R.P., Zanoni, T.A., van Beek, T.A., Posthumus, M.A., van de Haar, C., 1998. Essential leaf oil of Amyris diatrypa Sprengel from the Dominican Republic. J. Essent. Oil Res. 10, 175-178.
2. Adams, R.P., 1991. Cedarwood oil - analysis and properties. In: Linskens, H.-F., Jackson, J.F. (Eds.), Modern Methods of Plant Analysis, New Series, Vol. 12, Essential Oils and Waxes. Springer-Verlag, Berlin, pp. 159-173.
3. Adams, R.P., 1999. Systematics of multi-seeded eastern hemisphere Juniperus based on leaf essential oils and RAPD DNA fingerprinting. Biochem. Syst. Ecol. 27, 709-725.
4. Adams, R.P., 2000a. Systematics of smooth leaf margin Juniperus of the western hemisphere based on leaf essential oils and RAPD DNA fingerprinting. Biochem. Syst. Ecol. 28, 149-162.
5. Adams, R.P., 2000b. Systematics of Juniperus section Juniperus based on leaf essential oils and RAPD DNA fingerprinting. Biochem. Syst. Ecol. 28. 515-528.
6. Adams, R.P., 2000c. Systematics of the one seeded Juniperus of the eastern hemisphere based on leaf essential oils and random amplified polymorphic DNAs (RAPDs). Biochem. Syst. Ecol. 28, 529-543.
7. Adams, R.P., 2000d. The serrate leaf margined Juniperus (Section Sabina) of the western hemisphere: systematics and evolution based on leaf essential oils and Random Amplified Polymorphic DNAs (RAPDs). Biochem. Syst. Ecol. 28, 975-989.
8. Adams, R.P., 2001. Geographic variation in leaf essential oils and RAPDs of J. polycarpos K. Koch in central Asia. Biochem. Syst. Ecol. 29, 609-619.
9. Choi, J.-S., Yoon, N.-M., 1996. An excellent nickel boride catalyst for the selective hydrogenation of olefins. Synthesis 597-599.
10. 12-terpenoid dehydrogeosmin in flower heads of Rebutia marsoneri Werd. (Cactaceae). Helv. Chim. Acta 76, 2547-2552.
11. Jones, R.V.H., Sutherland, M.D., 1968. Terpenoid chemistry. XV. 1,5-Dimethylcyclodeca-1,5,7-triene, the precursor of geijerene in Geijera parviflora. Aust. J. Chem. 21, 2255-2274.
12. Kim, Y.-K., Cool, LG., Zavarin, E., 1994. cis-Calamenene-related sesquiterpenoids from Cupressus bakeri foliage. Phytochemistry 36, 961-965.
13. Tolstikov, G.A., Mikhailov, B.M., Dzhemilev, U.M., Dorokhov, V.A., Gubaidullin, L. Yu., & Zelinskii, N.D., 1980. Trans, trans, trans-1,5,9-trirnethyl-1,5,9-cyclodecatriene. USSR Patent SU 791717.
14. Wharton, P.S., Poon, Y.-C., Kluender, H.C., 1971. Conformational isomerism in dihydropregeijerene and hedycaryol. J. Org. Chem. 38, 735-740.