Two new sesquiterpenes (1–2), and one diterpene (3) were isolated from the roots of Salvia palaestina Bentham (Lamiaceae), together with eight known diterpenes and two triterpenes. Their structures were elucidated by 1D and 2D NMR spectroscopy, including 1D-TOCSY, DQF-COSY, ROESY, HSQC, and HMBC experiments, as well as ESIMS and chemical analysis.
FosterS, TylerVE. (2000) Tyler's Honest Herbal.The Haworth Press, Binghamton, New York, 327–330
2.
SteineggerE, HanselR. (1988) Lehrbuch der Pharmakognosie.Springer Verlag: Berlin
3.
Al-EisawiD. (1998) Field Guide to Wild Flowers of Jordan and neighbouring countries. Jordan Press Foundation Al-Rai, Amman, 175.
4.
MiskiM, UlubelenA, JohanssonC, MabryTJ. (1983) Antibacterial activity studies of flavonoids Salvia palaestina. Journal of Natural Products, 46, 874–875
5.
UlubelenA, MiskiM, JohanssonC, LeeE, MabryTJ, MatlinSA. (1985) Terpenoids from Salvia palaestina. Phytochemistry, 24, 1386–1387
6.
HusseinAA, de La TorreMC, RodriguezB, HammoudaFM, HussineyHA. (1997) Modified abietane diterpenoids and a methoxylupane derivative from Salvia palaestina. Phytochemistry, 45, 1663–1668
7.
HusseinAA, RodriguezB. (2000) A diterpenoid with a new modified abietane skeleton from Salvia palaestina. Zeitschrift fuer Naturforschung, B: Chemical Sciences, 55, 233–234.
8.
CioffiG, BaderA, MalafronteA, Dal PiazF, De TommasiN. (2008) Secondary metabolites from the aerial parts of Salvia palaestina. Phytochemistry, 69, 1005–1012
9.
MalafronteA, Dal PiazF, CioffiG, BracaA, LeoneA, De TommasiN. (2008) Secondary metabolites from the aerial parts of Salvia aethiopis L. Natural Product Communications3, 877–880
10.
De FeliceA, BaderA, LeoneA, SosaS, Della LoggiaR, TubaroA, De TommasiN. (2006) New polyhydroxylated triterpenes and anti-inflammatory activity of Salvia hierosolymitana. Planta Medica, 72, 643–649
11.
BisioA, De TommasiN, RomussiG. (2004) Diterpenoids from Salvia wagneriana. Planta Medica, 70, 452–457.
12.
ConnollyJD, HillRA. (1991) Dictionary of Terpenoids, vol. 2 Di- and higher terpenoids.Chapman & Hall: London
13.
KuoYH, YuMT. (1996) Diterpenes from the heartwood of Juniperus formosana Hay. var. concolor Hay. Chemical & Pharmaceutical Bulletin, 44, 1431–1435
14.
LinTC; FangJM, ChengYS. (1999) Terpenes and lignans from leaves of Chamaecyparis formosensis. Phytochemistry, 51, 793–801
15.
SanchezAJ, KonopelskiJP. (1994) The first synthesis of (±)-taxodone. Synlett5, 335–336
16.
BrunoM, SavonaG, PiozziF, De la TorreMC, RodriguezB, MarlierM. (1991) Abietane diterpenoids from Lepechinia meyeni and Lepechinia hastata. Phytochemistry, 30, 2339–2343
17.
RodriguezB. (2003) 1H and 13C NMR spectral assignments of some natural abietane diterpenoids. Magnetic Resonance in Chemistry, 41, 741–746
18.
NagyG, GuntherG, MatheI, BlundenG, YangMH, CrabbTA. (1999) 12-Deoxy-6,7-dehydroroyleanone, 12-deoxy-6-hydroxy-6,7-dehydroroyleanone and 12-deoxy-7,7-dimethoxy-6-ketoroyleanone from Salvia nutans roots. Phytochemitsry, 51, 809–812
19.
LinLZ, BlaskoG, CordellGA (1989) Diterpenes of Salvia prionitis. Phytochemistry, 28, 177–181.
20.
InagakiF, AbeA. (1985) Analysis of proton and carbon-13 nuclear magnetic resonance spectra of spathulenol by two-dimensional methods. Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry, 1773–1778
21.
ZetaderoC, BohlmannF, KingRM. (1992) Ent-labdanes manoyloxide and elipterol derivatives from Chrysocephalum ambiguum. Phytochemistry, 31, 1631–1638
22.
BozanB, OzturkN, KosarM, TunalierZ, BaserKHC. (2002) Antioxidant and free radical scavenging activities of eight Salvia species. Chemistry of Natural Compounds (Translation of Khimiya Prirodnykh Soedinenii), 38, 198–200.
