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1 .     22-Deacetyl A
C22H32O4     ÏàËÆ¶È:95.4%
Tetrahedron Letters          2005          46          5219-5223
First total synthesis of yanuthones: novel farnesylated epoxycyclohexenoid marine natural products
Goverdhan Mehta, Subhas Chandra Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     7-deacetoxyyanuthone A
C22H32O3     ÏàËÆ¶È:86.3%
Journal of Natural Products          2003          66          1499-1500
New Polyoxygenated Farnesylcyclohexenones, Deacetoxyyanuthone A and Its Hydro Derivative from the Marine-Derived Fungus Penicillium sp.
Xifeng Li, Hong Dae Choi, Jung Sook Kang, Chong-O. Lee, and Byeng Wha Son
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     yanuthone A
C24H34O5     ÏàËÆ¶È:83.3%
The Journal of Organic Chemistry          2000          65          7195-7200
Yanuthones: Novel Metabolites from a Marine Isolate of Aspergillus niger
Tim S. Bugni, Darren Abbanat, Valerie S. Bernan, William M. Maiese, Michael Greenstein, Ryan M. Van Wagoner, and Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Yanuthone A
C24H34O5     ÏàËÆ¶È:82.6%
Tetrahedron Letters          2005          46          5219-5223
First total synthesis of yanuthones: novel farnesylated epoxycyclohexenoid marine natural products
Goverdhan Mehta, Subhas Chandra Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     epi-yanuthone A
    ÏàËÆ¶È:73.9%
Tetrahedron Letters          2005          46          5219-5223
First total synthesis of yanuthones: novel farnesylated epoxycyclohexenoid marine natural products
Goverdhan Mehta, Subhas Chandra Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     epi-yanuthone C
    ÏàËÆ¶È:73.9%
Tetrahedron Letters          2005          46          5219-5223
First total synthesis of yanuthones: novel farnesylated epoxycyclohexenoid marine natural products
Goverdhan Mehta, Subhas Chandra Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     22-deacetyl-epi-yanuthone A
    ÏàËÆ¶È:72.7%
Tetrahedron Letters          2005          46          5219-5223
First total synthesis of yanuthones: novel farnesylated epoxycyclohexenoid marine natural products
Goverdhan Mehta, Subhas Chandra Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (2Z,6E,10E)-6,10-Dimethyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-triene-1,12-diol
C20H34O2     ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          2001          9          1781-1791
Synthesis of Plaunotol Derivatives and their Antibacterial Activities against Helicobacter pylori
Keiko Tago, Emiko Minami, Kayoko Masuda, Toshiyuki Akiyama, Hiroshi Kogen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1-hydroxyyanuthone A
C24H34O6     ÏàËÆ¶È:70.8%
The Journal of Organic Chemistry          2000          65          7195-7200
Yanuthones: Novel Metabolites from a Marine Isolate of Aspergillus niger
Tim S. Bugni, Darren Abbanat, Valerie S. Bernan, William M. Maiese, Michael Greenstein, Ryan M. Van Wagoner, and Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     elegandiol
C20H34O2     ÏàËÆ¶È:68.1%
Journal of Natural Products          1998          61          92-95
Studies on the Synthesis of Elegan-Type Linear Diterpenes: The Efficient Total Syntheses of Eleganolone, Eleganolone Acetate, Elegandiol, Eleganonal, and Epoxyeleganolone
Jing Li, Jiong Lan, Zuosheng Liu, and Yulin Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     eleganediol
    ÏàËÆ¶È:68.1%
Phytochemistry          1999          52          1447-1454
Geranylgeraniol-derived diterpenoids from the brown alga Bifurcaria bifurcata
Gerald Culioli, Mohamed Daoudi, Veronique Mesguiche, Robert Valls, Louis Piovetti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     diol (2E,6E,10E)-3-hydroxymethyl-7,11,15-trimethylhexadeca-2,6,10,14-tetraen-l-ol
    ÏàËÆ¶È:68.1%
Journal of Natural Products          1990          Vol 53          845
Tropical Marine Algae, VII. The Chemical Composition of Marine Algae from North Queensland Waters
Anthony D. Wright, John C. Coll, Ian R. Price
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (S)-13-hydroxygeranylgeraniol
    ÏàËÆ¶È:68.1%
Phytochemistry          1995          39          145-149
(S)-13-hydroxygeranylgeraniol-derived furanoditerpenes from Bifurcaria bifurcata
Robert Valls, Louis Piovetti, Bernard Banaigs, Albert Archavlis, Max Pellegrini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4-(hydroxy-5(E,E-farnesyl)benzoic acid
C22H3003     ÏàËÆ¶È:68.1%
Phytochemistry          1987          26          2367-2370
New prenylated phenolics from Piper auritum
Stephen A. Ampofo,Vassilios Roussis,David F. Wiemer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     all-E-geranylgeraniol
C20H34O     ÏàËÆ¶È:68.1%
Phytochemistry          1989          28          3159-3162
Terpenoids and an apocarotenoid from seeds of Bixa orellana
Isaac J.O. Jondiko,Gerald Pattenden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (10R,11R)-(+)-qualene-10,11-epoxide
    ÏàËÆ¶È:68.1%
Tetrahedron letters          1982          23          5413-5414
(10R̃, 11R̃-(+)-squalene-10, 11-epoxide: Isolation from Laurencia okamurai and the asymmetric synthesis
Hideo Kigoshi, Makoto Ojika, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1'elegandeiol
    ÏàËÆ¶È:68.1%
Tetrahedron letters          1980          21          1849-1852
Epoxyeleganolone et eleganediol, deux nouveaux diterpenes de bifurcaria bifurcata ross (cystoseiracees)
J.F. Biard, J.F. Verbist, R Floch, Y Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Ethyl 2-(diethoxyphosphinyl)-5,9,13-trimethyl-(E,E,E)-4,8,12-tetradecatrienoate
C23H42O5P     ÏàËÆ¶È:68.1%
Bioorganic & Medicinal Chemistry          1998          6          687-694
Phosphonate and bisphosphonate analogues of farnesyl pyrophosphate as potential inhibitors of farnesyl protein transferase
Sarah A Holstein, Diana M Cermak, David F Wiemer, Kriste Lewis, Raymond J Hohl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (2E,10E)-3,7,11,15-tetramethylhexadeca-2,10,14-trien-1-ol
C20H36O     ÏàËÆ¶È:68.1%
Bioorganic & Medicinal Chemistry          2010          18          3116-3124
Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines
Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (10R,11R)-(+)-squalene-10,11-epoxide
C30H50O     ÏàËÆ¶È:68.1%
Tetrahedron          1986          42          3789-3792
Isolation of (10R,11R)-(+)-squalene-10,11-epoxide from the red alga laurencia okamurai and its enantioselective synthesis
Hideo Kigoshi, Makoto Ojika, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-farnesyl-2-hydroxy benzoic acid
C22H30O3     ÏàËÆ¶È:68.1%
Journal of Ethnopharmacology          2006          103          461-467
3-Farnesyl-2-hydroxybenzoic acid is a new anti-Helicobacter pylori compound from Piper multiplinervium
T. R¨¹egg, A.I. Calder¨®n, E.F. Queiroz, P.N. Sol¨ªs, A. Marston, F. Rivas, E. Ortega-Barr¨ªa, K. Hostettmann, M.P. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     luffarin-Q
C25H38O2     ÏàËÆ¶È:68.1%
Australian Journal of Chemistry          1992          45          1705-1743
The Luffarins (A-Z), Novel Terpenes From an Australian Marine Sponge, Luffariella geometrica
MS Butler and RJ Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     2-Farnesyl-3,4-dihydroxybenzoic acid
C22H30O4     ÏàËÆ¶È:68.1%
Phytochemistry          2011          72          238-241
Prenylhydroxybenzoic acid compounds with pungent activity from Piper arieianum (CDC) leaves
Edwin Correa, Olov Sterner, Fernando Echeverri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (2Z)-[(3E,7E)-4,8,12-Trimethyltrideca-3,7,11-trienyl]but-2-ene-1,4-diol
C20H34O2     ÏàËÆ¶È:68.1%
Bioorganic & Medicinal Chemistry          2001          9          1781-1791
Synthesis of Plaunotol Derivatives and their Antibacterial Activities against Helicobacter pylori
Keiko Tago, Emiko Minami, Kayoko Masuda, Toshiyuki Akiyama, Hiroshi Kogen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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