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²éѯ½á¹û£º¹²²éµ½143¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7¦Â,12¦Á-dihydroxy-13-epi-manoyl oxide C20H34O3 ÏàËÆ¶È:100% Planta Medica 2009 75 1344-1348 Terpenoids from Roots of Chloranthus henryi Xianwen Gan, LeiMa, Qigang Chen, Qiuqun Chen, Qiang Yu, Lihong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 12¦Á-hydroxy-13-epi-manoyloxide C24H34O2 ÏàËÆ¶È:75% Phytochemistry 1995 40 1201-1207 Diterpenoids from Grindelia tarapacana Lin Zhou, Eduardo R. Fuentes, Joseph J. Hoffmann, Barbara N. Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ent-7¦Â,12¦Á-dihydroxy-3-oxo-13-epi-manoyl oxide ÏàËÆ¶È:75% Phytochemistry 1995 38 1237-1244 Preparation of polyoxygenated ent-13-epi-manoyl oxides by chemical-microbiological semisyntheses Andr¨¦s Garc¨ªa-Granados, Emilio Liñ¨¢n, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 12¦Á-hydroxy-13-epi-manolyoxide C20H34O2 ÏàËÆ¶È:75% Phytochemistry 1991 30 2991-3000 Diterpenes and norditerpenes from the Aristeguetia group C. Zdero, F. Bohlmann, R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . varol(ent-12¦Á-hydroxy-13-epi-manoyl oxide) ÏàËÆ¶È:75% Phytochemistry 1989 28 1851-1854 The microbiological transformation of some ent-13-epi-manoyl oxide diterpenes by Gibberella fujikuroi Braulio M. Fraga,pedro Gonz¨¢lez,Ricardo Guillermo,Melchor G. Hern¨¢ndez,Juana Rovirosa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ent-7¦Â,12¦Á,19-trihydroxy-13-epi-maoyl oxide C20H34O4 ÏàËÆ¶È:75% Phytochemistry 1989 28 1851-1854 The microbiological transformation of some ent-13-epi-manoyl oxide diterpenes by Gibberella fujikuroi Braulio M. Fraga,pedro Gonz¨¢lez,Ricardo Guillermo,Melchor G. Hern¨¢ndez,Juana Rovirosa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . varol ÏàËÆ¶È:75% Phytochemistry 1985 24 1789-1792 Diterpenoids from Sideritis varoi subspecies cuatrecasasii: 13C NMR of ent-13-epi-manoyl oxides functionalized at C-12 A. Garc¨ªa-Granados, A. Mart¨ªnez, A. Molina, M.E. Onorato, M. Rico, A.Saenz de Buruaga, J.M.Saenz de Buruaga Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (12S,13R)-8,12-epoxy-14-labden-12-ol ÏàËÆ¶È:75% Acta Chemica Scandinavica 1978 32B 310-312 Tobacco Chemistry. 46. Syntheses of (12R,13S)- and (12S,13R)-8,12-Epoxy-14-labden-13-ol and (12S,13R)-8,13-Epoxy-14-labden-12-ol, Three Tobacco Diterpenoids. Wahlberg, Inger; Curvall, Margareta; Enzell, Curt R. Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ent-3¦Â,7¦Â,12¦Á-Trihydroxy-13-epi-manoyl oxide ÏàËÆ¶È:70% Phytochemistry 1995 38 1237-1244 Preparation of polyoxygenated ent-13-epi-manoyl oxides by chemical-microbiological semisyntheses Andr¨¦s Garc¨ªa-Granados, Emilio Liñ¨¢n, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . varodiol (ent-3¦Â,12¦Á-dihydroxy-13-epi-manoyl oxide ) C19H31O3 ÏàËÆ¶È:70% Phytochemistry 1989 28 1851-1854 The microbiological transformation of some ent-13-epi-manoyl oxide diterpenes by Gibberella fujikuroi Braulio M. Fraga,pedro Gonz¨¢lez,Ricardo Guillermo,Melchor G. Hern¨¢ndez,Juana Rovirosa Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . varodiol ÏàËÆ¶È:70% Phytochemistry 1985 24 1789-1792 Diterpenoids from Sideritis varoi subspecies cuatrecasasii: 13C NMR of ent-13-epi-manoyl oxides functionalized at C-12 A. Garc¨ªa-Granados, A. Mart¨ªnez, A. Molina, M.E. Onorato, M. Rico, A.Saenz de Buruaga, J.M.Saenz de Buruaga Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . coleol ÏàËÆ¶È:70% Magnetic Resonance in Chemistry 1988 26 117-119 Carbon-13 and proton two-dimensional NMR study of diterpenoids of Coleus forskohlii Om Prakash, Raja Roy, J. S. Tandon and M. M. Dhar Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7¦Â-hydroxymanoyl oxide C20H34O2 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 2005 53(3) 286-289 Five New Diterpenoids from the Bark of Taiwania cryptomerioides Chi-I CHANG,Mei-Huims TSENG,and Yueh-Hsiung KUO Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Â,12¦Â-dihydroxy-ent-13-epi-manoyl oxide C20H34O3 ÏàËÆ¶È:65% Phytochemistry 2003 67-70 The biotransformation of the diterpene 2¦Â-hydroxy-ent-13-epimanoyl oxide by Gibberella fujikuroi Braulio M. Fraga, Pedro Gonz¨¢lezb, Melchor G. Hern¨¢ndeza, Sergio Su¨¢rez Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 8(9),15-Isopimaradien-3¦Â-ol C20H32O ÏàËÆ¶È:65% Journal of Natural Products 2004 67 631-637 Labdanes and Isopimaranes from Platycladus orientalis and Their Effects on Erythrocyte Membrane and on Plasmodium falciparum Growth in the Erythrocyte Host Cells Javad Asili, Maja Lambert, Hanne L. Ziegler, , Majid Sairafianpour, Matthias Witt, Gholamreza Asghari, Ismaiel S. Ibrahimi, and Jerzy W. Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1¦Â,16¦Á,17-trihydroxy-ent-kaurane C20H34O3 ÏàËÆ¶È:65% Planta Medica 2004 70 540-550 Structure of Kaurane-Type Diterpenes from Parinari sprucei and their Potential Anticancer Activity Alessandra Braca,Annahil Armenise, Ivano Morelli,Jeannette Mendez,Qiuwen Mi,Hee-Byung Chai,Steven M. Swanson ,A. Douglas Kinghorn,Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ent-3-oxo-13-epi-manoyl oxide C20H32O2 ÏàËÆ¶È:65% Phytochemistry 2000 55 891-901 Five diterpenoids (agallochins A-E) from the mangrove plant Excoecaria agallocha Linn Ammanamanchi S.R. Anjaneyulu , Vadali Lakshmana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ribenone ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1996 44 2100-2102 Chemical Structures of Excoecarins A, B and C : Three New Labdane-Type Diterpenes from Wood, Excoecaria agallocha Tenji KONISHI,Shiu KIYOSAWA,Takao KONOSHIMA and Yasuhiro FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ribenone C20H32O2 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1996 44 229-231 Three New Labdane-Type Diterpenes from Wood, Excoecaria agallocha Tenji KONISHI,Masuji AZUMA,Rie ITOGA,Shiu KIYOSAWA,Yasuhiro FUJIWARA and Yasuo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ribenone ÏàËÆ¶È:65% Journal of Asian Natural Products Research 2005 7 729-734 A new isopimarane-type diterpene and a new natural atisanetype diterpene from Excoecaria agallocha JIE KANG, RUO-YUN CHEN and DE-QUAN YU Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ribenone C20H34O4 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1998 46 1393-1398 Five New Labdane-Type Diterpenes from Excoecaria agallocha. IV Tenji KONISHI,Yasuhiro FUJIWARA,Takao KONOSHIMA and Shiu KIYOSAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ribenone ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1998 46 721-722 Stereostructure of Excoecarin H, a Novel seco-Labdane-Type Diterpene from Excoecaria agallocha Tenji KONISHI,Takao KONOSHIMA,Yasuhiro FUJIWARA and Shiu KIYOSAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . jolkinolide E C20H28O2 ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 1995 20 169-170 Studies on the Chemical Constituents of Euphorbia nematocypha Hand.-Mazz Zhao Kuijun, Liu Suolan, Yang Jun and Li Xiuqing , Xu Guojun, Jin Rongluan and Xu Luoshan Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ent-hurane-7¦Á,16¦Â,17-triol C20H34O3 ÏàËÆ¶È:65% Journal of Natural Products 1992 Vol 55 1477 Diterpenes of Calibrachoa parviflora Carl A. Elliger, Rosalind Y. Wong, Mabry Benson, William Gaffield, Anthony C. Waiss Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . ribenone ÏàËÆ¶È:65% Phytochemistry 1995 38 1237-1244 Preparation of polyoxygenated ent-13-epi-manoyl oxides by chemical-microbiological semisyntheses Andr¨¦s Garc¨ªa-Granados, Emilio Liñ¨¢n, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . ribenone ÏàËÆ¶È:65% Phytochemistry 1994 37 741-747 Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities Andr¨¦s Garc¨ªa-Granados, M Belinda Jim¨¦nez, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ent-7¦Á,16¦Â,17-Trihydraxykarrrane 17-acetate ÏàËÆ¶È:65% Phytochemistry 1994 37 717-721 The microbiological transformation of two ent-16¦Â, 17-epoxykaurane derivatives by Gibberella fujikuroi Braulio M. Fraga, Pedro Gonz¨¢lez, Ricardo Guillermo, James R. Hanson, Melchor G. Hern¨¢ndez, Jacqueline A. Takahashi Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ent-7¦Á,16¦Â,17-Trihydraxykarrrane 7¦Â,17-diacetate C22H34O3 ÏàËÆ¶È:65% Phytochemistry 1994 37 717-721 The microbiological transformation of two ent-16¦Â, 17-epoxykaurane derivatives by Gibberella fujikuroi Braulio M. Fraga, Pedro Gonz¨¢lez, Ricardo Guillermo, James R. Hanson, Melchor G. Hern¨¢ndez, Jacqueline A. Takahashi Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 2 ÏàËÆ¶È:65% Chemical Research in Chinese Universities 2007 23 541-543 New ent-Isopimarane Diterpene from Mangrove Excoecaria agallocha L. LIXiang, LEI Jun, ZHENG Yi-nan, Sattler Isabel and LIN Wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . coleol ÏàËÆ¶È:65% Phytochemistry 1989 28 859-862 Minor diterpenoids of Coleus forskohlii Bruno Gabetta,Gianfranco Zini,Bruno Danieli Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 8,13-epoxy-labd-14-en-11-one ÏàËÆ¶È:65% Phytochemistry 1989 28 859-862 Minor diterpenoids of Coleus forskohlii Bruno Gabetta,Gianfranco Zini,Bruno Danieli Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ent-7¦Â,8¦Á-dihydroxylabda-13(16),14-diene C20H34O2 ÏàËÆ¶È:65% Heterocycles 2005 65 809-822 New Labdane-Type Diterpenoids from Croton oblongifolius and Their Cytotoxic Activity Chaiyo Chaichantipyuth,* Amorn Petsom, Pagorn Taweechotipatr, Nongnuj Muangsin, Narongsak Chaichit, Songchan Puthong, Sophon Roengsumran, Masatoshi Kawahata, Toshiko Watanabe, and Tsutomu Ishikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 6¦Á-hydroxygrindelic acid C20H32O4 ÏàËÆ¶È:65% Phytochemistry 1981 20 2249-2253 Grindelane diterpenoid acids from Grindelia humilis: Feeding deterrency of diterpene acids towards aphids Allan F. Rose, Kenneth C. Jones, W.F. Haddon, David L. Dreyer Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . sterebin D C18H30O3 ÏàËÆ¶È:65% Tetrahedron 1986 42 6443-6446 Sterebins A, B, C and D, bisnorditerpenoids of stevia rebaudiana leaves Yoshiteru Oshima, Jun-ichi Saito, Hiroshi Hikino Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 57 ÏàËÆ¶È:65% Natural Product Communications 2008 3 399-412 Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . heteroscyphin B C20H30O3 ÏàËÆ¶È:65% Journal of Natural Products 2014 77 1336-1344 Diterpenoids from the Chinese Liverwort Heteroscyphus tener and Their Antiproliferative Effects Zhao-Min Lin, Yan-Xia Guo, Shu-QI Wang, Xiao-Ning Wang, Wen-Qiang Chang, Jin-Chuan Zhou, Huiqing Yuan, and Hongxiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3-acetylvarodiol ÏàËÆ¶È:63.6% Phytochemistry 1994 37 741-747 Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities Andr¨¦s Garc¨ªa-Granados, M Belinda Jim¨¦nez, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 3-acetylvarodiol ÏàËÆ¶È:63.6% Phytochemistry 1985 24 1789-1792 Diterpenoids from Sideritis varoi subspecies cuatrecasasii: 13C NMR of ent-13-epi-manoyl oxides functionalized at C-12 A. Garc¨ªa-Granados, A. Mart¨ªnez, A. Molina, M.E. Onorato, M. Rico, A.Saenz de Buruaga, J.M.Saenz de Buruaga Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . ent-16¦Â-hydroxy-17-acetoxy-kauran-19-al ÏàËÆ¶È:63.6% Qu¨ªmica Nova 2012 35 1570-1576 Ent-kaurane diterpenoids and other constituents from the stem of Xylopia laevigata (Annonaceae) Silva, Dayanne Meneses; Costa, Emmanoel Vilaça; Nogueira, Paulo Cesar de Lima; Moraes, Val¨¦ria Regina de Souza; Cavalcanti, S¨®crates Cabral de Holanda; Salvador, Marcos Jos¨¦; Ribeiro, Luis Henrique Gonzaga; Gadelha, Fernanda Ramos; Barison, Andersson; Fer Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . heteroscyphin D C22H37O5N ÏàËÆ¶È:63.6% Journal of Natural Products 2014 77 1336-1344 Diterpenoids from the Chinese Liverwort Heteroscyphus tener and Their Antiproliferative Effects Zhao-Min Lin, Yan-Xia Guo, Shu-QI Wang, Xiao-Ning Wang, Wen-Qiang Chang, Jin-Chuan Zhou, Huiqing Yuan, and Hongxiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . compound 21 ÏàËÆ¶È:61.9% Phytochemistry 1990 29 2169-2174 Terpenoids from some Japanese liverworts Fumihiro Nagashima,Masao Toyota,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . Compound 3 C21H28O3 ÏàËÆ¶È:61.9% Magnetic Resonance in Chemistry 2005 43 97-99 Structural and spectral assignment by two-dimensional NMR of two new derivatives of the abietane diterpenoid taxodione Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . me tucumanate ÏàËÆ¶È:61.9% Phytochemistry 1985 24 787-790 A diterpene acid from baccharis tucumanensis P. C. Rossomando, O. S. Giordano, J. Espiñeira, P. Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . me tucumanate ÏàËÆ¶È:61.9% |

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