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²éѯ½á¹û£º¹²²éµ½631¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 1 ÏàËÆ¶È:80% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 1 ÏàËÆ¶È:73.3% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (-)-ledol C15H26O ÏàËÆ¶È:73.3% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 1b ÏàËÆ¶È:73.3% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 1c ÏàËÆ¶È:73.3% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (-)-10(R)-hydroxyalloaromadendrane C15H26O ÏàËÆ¶È:73.3% Tetrahedron 1996 52 2359-2368 Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa Hiroshi Hirota, Yasuhiko Tomono, Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 5(9),6-tricyclohumulan-4¦Á,8¦Á-diol C15H26O2 ÏàËÆ¶È:73.3% Zeitschrift f¨¹r Naturforschung C 2002 57 680-685 Microbial Conversion of Partheniol by Calonectria decora G. T. Maatooq Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . pubinernoid C C15H26O2 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2006 Vol. 89 1169 Three Novel Terpenoids from Schisandra pubescens var. pubinervis Sheng-Xiong Huang, Jing Yang, Wei-Lie Xiao, Yan-Ling Zhu, Rong-Tao Li, Li-Mei Li, Jian-Xin Pu, Xian Li, Sheng-Hong Li, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (-)-epi-cedrol ÏàËÆ¶È:66.6% Phytochemistry 2003 64 303-323 Terpenoids from the seeds of Artemisia annua Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (4R,5R,8S)-4,5-epoxycaryophyllan-8-ol C15H26O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1999 62 41-44 Biotransformation of Caryophyllene Oxide by Botrytis cinerea Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . D-aromadendrane-4¦Â, 10¦Á-diol C15H26O2 ÏàËÆ¶È:66.6% Acta Botanica Yunnanica 2002 24(1) 129-132 Sesquiterpenoids from Michelia lacei and Their Chemotaxonomic Significance CHENG Yong-Xian,LEI Mao-Lin,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 1 ÏàËÆ¶È:66.6% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 6-isocedrol ÏàËÆ¶È:66.6% Journal of Natural Products 1984 Vol 47 924-933 13C-nmr Study of Cedrol, 6-Isocedrol, and ¦Á-Cedrene P. Joseph-Nathan, R. L. Santillan, A. Guti¨¦rrez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 6-isocedrol ÏàËÆ¶È:66.6% Journal of Natural Products 1986 Vol 49 79 13C-nmr Studies of Cedranolides P. Joseph-Nathan, A. Guti¨¦rrez, J. D. Hern¨¢ndez, L. U. Rom¨¢n, R. L. Santillan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Cedran-3¦Á-ol ÏàËÆ¶È:66.6% Phytochemistry 1996 41 1361-1365 Terpenes from heartwood of Juniperus chinensis Jim-Min Fang, Ying-Chih Chen, Beng-Wern Wang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (+)-11-epispathulenol ÏàËÆ¶È:66.6% Phytochemistry 1995 40 827-831 Sesquiterpenes and geranylgeranylglycerol from the brown algae Taonia lacheana and Taonia atomaria f. ciliata: their chemotaxonomic significance Corrado Tringali, Mario Piattelli, Carmela Spatafora Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 8-Epicedrol ÏàËÆ¶È:66.6% Phytochemistry 1995 39 1081-1084 The biotransformation of 8-epicedrol and some relatives by Cephalosporium aphidicola Estelle Gand, James R. Hanson, Habib Nasir Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 11-hydroxy-4-amorphen-15-oic acid C15H24O3 ÏàËÆ¶È:66.6% Phytochemistry 1994 35 425-433 The sesquiterpenes of Fabiana imbricata Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 11-dihydroxyguaiane C15H26O ÏàËÆ¶È:66.6% Phytochemistry 1994 36 695-698 Sesquiterpenes and other constituents from chilean mutisieae M. Bittner, M. Silva, Z. Rozas, F. Papastergiou, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (-)-ledol C15H26O ÏàËÆ¶È:66.6% Phytochemistry 1993 32 478-480 Phenylpropanoids and (− -ledol from two Piper species S. K. Koul, S. C. Taneja, S. Malhotra, K. L. Dhar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 12 ÏàËÆ¶È:66.6% Phytochemistry 1987 26 1059-1063 Sesquiterpene lactones and a sesquiterpene diol from jamaican ambrosia peruviana Gwendolyn Goldsby,Basil A. Burke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . Compound 10 ÏàËÆ¶È:66.6% Magnetic Resonance in Chmesitry 2003 41 1034-1037 Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Trichodone B C15H26O3 ÏàËÆ¶È:66.6% Chemistry & Biodiversity 2012 9 1205-1212 Sesquiterpenes and Cyclopeptides from the Endophytic Fungus Trichoderma asperellumSamuels, Lieckf. & Nirenberg Gang Ding, Amanda Juan Chen, Jin Lan, Hongwu Zhang, Xiangdong Chen, Xingzhong Liu and Zhongmei Zou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4-Muurolen-7,15-diol, 7,15-carbonate C15H24O ÏàËÆ¶È:62.5% Phytochemistry 1994 35 425-433 The sesquiterpenes of Fabiana imbricata Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . compound 14 ÏàËÆ¶È:61.1% Phytochemistry 1990 29 2597-2603 Fusicoccane-,dolabellane-and rearranged labdane-type diterpenoids from the liverwort Pleurozia gigantea Yoshinori Asakawa,Xuehuilin Lin,Motoo Tori,Keiko Kondo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . spathulenol ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(10) 1208-1210 A New Furanoid Diterpene from Caesalpinia pulcherrima Consolacion Y. RAGASA,Jerome GANZON,Joy HOFILEÑA,Benjie TAMBOONG,and John A. RIDEOUT Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . pipelol A C15H26O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2002 50(10) 1413-1415 New Megastigmane Glycoside and Aromadendrane Derivative from the Aerial Part of Piper elongatum Chikako MASUOKA,Masateru ONO, Yasuyuki ITO,Masafumi OKAWA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . acomadendrane-4¦Â,10¦Â-diol C15H26O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2000 48(3) 357-361 The Constituents of the Root and Stem of Aristolochia heterophylla Hemsl Tian-Shung Wu ,Yu-Yi CHAN ,and Yann-Lii LEU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (13S,14S)-Ent-13,14-epoxy-5-epi-verticillol C20H34O2 ÏàËÆ¶È:60% Phytochemistry 2005 66 1662-1670 ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . (-)-aristol-1(10)-en-12-ol C15H24O ÏàËÆ¶È:60% Phytochemistry 2003 581-587 Sesquiterpene constituents from the liverwort Bazzania japonica Runhua Lu, Claudia Paul, Simla Basar, Wilfried A. König,Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . 15-nor-10-hydroxy-oplopan-4-oic acid C14H24O2 ÏàËÆ¶È:60% Phytochemistry 2003 64 303-323 Terpenoids from the seeds of Artemisia annua Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . aromadendr-1(10)-en-9-one ÏàËÆ¶È:60% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . squamulosone ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . (1S,10S)-9¦Á-hydroxy-allo-aromadendrane C15H26O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (1R,10R)-9¦Â-hydroxyaromadendrane C15H26O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . 2¦Â,9¦Â-dihydroxyaromadendr-1(10)-ene C15H24O2 ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . 2¦Â,9¦Á-dihydroxyaromadendr-1(10)-ene C15H24O2 ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . axinysone C C15H22O3 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(12) 2004-2010 Sesquiterpenes from the Sponge Axinyssa isabela Eva Zub¨ªa, Mar¨ªa J. Ortega, and J. Luis Carballo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . pulicanadienal A C15H24O3 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 523-531 Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities Jorge Triana, Mariana Lpez, Francisco J. Prez, Javier Gonzlez-Platas,Jos Quintana, Francisco Estvez, Francisco Len, and Jaime Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . pulioplopanone B C15H26O3 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 523-531 Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities Jorge Triana, Mariana Lpez, Francisco J. Prez, Javier Gonzlez-Platas,Jos Quintana, Francisco Estvez, Francisco Len, and Jaime Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . comound 3 C15H24O ÏàËÆ¶È:60% Journal of Natural Products 2004 67 577-583 New Marine Sesquiterpenoids and Diterpenoids from the Okinawan Soft Coral Clavularia koellikeri Kazuo Iguchi, Takashi Fukaya, Akiko Yasumoto, and Kinzo Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . methyl 2-[2-(tert-butyldimethylsilyl)oxypropionyloxy]-3-methylpentanoate C16H32O5Si ÏàËÆ¶È:60% Journal of Natural Products 2007 70 1073-1083 Antineoplastic Agents. 561. Total Synthesis of Respirantin George R. Pettit,Thomas H. Smith, Song Feng, John C. Knight, Rui Tan, Robin K. Pettit, and Peter A. Hinrichs Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . (4Z,3S,8¦Á,11S)-caryophyll-4(5)-ene-3,8,14-triol ÏàËÆ¶È:60% Journal of Natural Products 2000 63 44-47 Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . (8R)-8-hydroxypatchoulol C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 1999 62 437-440 Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 4¦Á-methylcadinane-4¦Á-methyl-1¦Á,2¦Á,10¦Á-triol C15H28O3 ÏàËÆ¶È:60% Journal of Natural Products 1997 60 38-40 Bioactive Compounds from Taiwania cryptomerioides Kan He, Lu Zeng, Guoen Shi, Geng-Xian Zhao, John F. Kozlowski, and Jerry L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . 4¦Â,10¦Á-aromadendranediol C15H26O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1989 37 509-510 Studies on the Sequiterpenoids of Panax ginseng C. A. MEYER. III Hisakatsu IWABUCHI,Masahiro YOSHIKURA and Wasuke KAMISAKO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . ent-oplopanone C15H26O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . 4,10-epi-5¦Â-hydroxydihydroeudesmol C15H28O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1987 35 1460-1463 Novel Eudesmane-Type Sesquiterpenes from Alpinia japonica (THUNB.) MIQ HIDEJI ITOKAWA,HIROSHI MORITA and KINZO WATANABE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . 4¦Â,10¦Â-Aromadendranediol ÏàËÆ¶È:60% Journal of Chinese Pharmaceutical Sciences 2009 18 146-150 Chemical constituents isolated from Saruma henryi Shi-Wen Dong; Ming-Ying Shang; Xuan Wang; Shu-Xiang Zhang; Chen Li; Shao-Qing Cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . spathulenol [10(14)-aromadendren-4-ol] ÏàËÆ¶È:60% Biochemical Systematics and Ecology 2002 30 493-495 Spathulenol: a rare sesquiterpene from soft coral Sinularia kavarattiensis T. Venkateshwar Goud, N. Srinivasa Reddy, P. Krishnaiah, Y. Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . Ent-spathulenol C15H24O ÏàËÆ¶È:60% Guihaia 2009 29 272-274 Study on terpenoid from the roots of Croton crassifolius YANG Xian-Hui; CHEN Shang-Wen; LIN Qiang; DENG Shi-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ |

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3Â¥2012-08-24 11:23:17













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-ledol from two Piper species
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