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190824656: ½ð±Ò+10 2014-08-25 20:47:03
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190824656: ½ð±Ò+10 2014-08-25 20:47:03
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½760¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 synthesisHideo Kigoshi, Makoto Ojika, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada Structure 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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-(+)-squalene-10, 11-epoxide: Isolation from Laurencia okamurai and the asymmetric synthesis