Open Access. Powered by Scholars. Published by Universities.®

Physical Sciences and Mathematics Commons

Open Access. Powered by Scholars. Published by Universities.®

TÜBİTAK

Journal

2002

Labiatae

Articles 1 - 2 of 2

Full-Text Articles in Physical Sciences and Mathematics

Phenolic Constituents From Phlomis Lycia, İclal Saracoğlu, Ü. Şebnem Harput, İhsan Çaliş, Yukio Ogihara Jan 2002

Phenolic Constituents From Phlomis Lycia, İclal Saracoğlu, Ü. Şebnem Harput, İhsan Çaliş, Yukio Ogihara

Turkish Journal of Chemistry

From the aerial parts of Phlomis lycia L. (Labiatae) a lignan glucoside, (-)-dihydrodehyrodiconiferyl alcohol-9-O-\beta -D-glucopyranoside (1); a caffeic acid ester, chlorogenic acid (2); three phenylethanoid glycosides, forsythoside B (3), alyssonoside (4) and leucosceptoside B(5); and two iridoid glucosides, lamiide (6) andauroside (7), were isolated. The structure elucidation of the isolated compounds was carried out by spectroscopic (UV, IR, 1D- and 2D-NMR, FAB-MS) methods. (-)-Dihydrodehyrodiconiferyl alcohol-9-O-\beta -D-glucopyranoside (1) and chlorogenic acid (2) were isolated for the first time from Phlomis species in this study.


Diterpenes From Sideritis Sipylea And S. Dichotoma, Gülaçti Topçu, Ahmet C. Gören, Turgut Kiliç, Y. Kemal Yildiz, Gülendam Tümen Jan 2002

Diterpenes From Sideritis Sipylea And S. Dichotoma, Gülaçti Topçu, Ahmet C. Gören, Turgut Kiliç, Y. Kemal Yildiz, Gülendam Tümen

Turkish Journal of Chemistry

Two Sideritis species afforded eleven kaurene and one beyerene diterpenes. Structures of the compounds from Sideritis sipylea} were elucidated as linearol (1), 7-epicandicandiol (2), sideridiol (3), siderol (4), isolinearol (5), isosidol (6) and epoxyisolinearol (7). Linearol was treated with m -chloroperbenzoic to afford its analogues ent-3\beta ,7\alpha ,17-trihydroxy-18-acetoxykaur-15-ene (1a) and ent}-7\alpha ,17,18-trihydroxy-3\beta -acetoxykaur-15-ene (1b) as new compounds. From the second species, Sideritis dichotoma, the kaurenes sideridiol (3) siderol (4), ent-7\alpha ,18-dihydroxy-15\beta ,16\beta -epoxykaurane (8)}, ent}-7\alpha -acetoxy,18-hydroxy-15\beta ,16\beta -epoxykaurane (9), ent-7\alpha -acetoxy-15,18-dihydroxy-kaur-16-ene (10), ent-7\alpha ,15,18-trihydroxykaur-16-ene (11) and the beyerene ent-7\alpha ,18-dihydroxybeyer-15-ene (12) were isolated. Structural elucidation is based on NMR techniques …