| ²é¿´: 280 | »Ø¸´: 1 | |||
mojiaoliгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
| 9.5,15.1,19.7,20.2,21.6,22.4,23.4,33.9,35.6,38.8,42.9,46.2,50.2,76.8,77.8,128.9,129.4,131.7,132.5,134.4,135.0 |
» ²ÂÄãϲ»¶
332Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ29È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ14È˻ظ´
291 Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
»úеר˶270Çóµ÷¼Á£¬½ÓÊÜ¿çרҵ
ÒѾÓÐ11È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
±¾¿Æ211 ¹¤¿Æ085400 280·ÖÇóµ÷¼Á ¿É¿çרҵ
ÒѾÓÐ8È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ23È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ15È˻ظ´
269Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ70%£©
ÒѾÓÐ8È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¿û»¨ÅɸßÊÖ
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 40 (СѧÉú)
- ½ð±Ò: 29.8
- É¢½ð: 20
- ºì»¨: 2
- Ìû×Ó: 229
- ÔÚÏß: 99.8Сʱ
- ³æºÅ: 2513202
- ×¢²á: 2013-06-19
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
mojiaoli: ½ð±Ò+10 2015-01-27 18:38:07
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
mojiaoli: ½ð±Ò+10 2015-01-27 18:38:07
|
1 . (1S,4R,13S)-Ethoxycembra-2(E),7(E),11(E)-trien-4-ol C20H36O2 ÏàËÆ¶È:80.9% Chemistry of Natural Compounds 2007 43 143-148 SYNTHESIS OF N-METHYL UROCANATES OF HYDROXYDERIVATIVES OF ISOCEMBROL F. A. Valeev,1 Sh. M. Salikhov,O. Yu. Krasnoslobodtseva,B. T. Sharipov L. V. Spirikhin, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (1S,4R,13S)-cembra-2(E),7(E),11(E)-trien-4,13-diol C20H36O2 ÏàËÆ¶È:76.1% Chemistry of Natural Compounds 2007 43 143-148 SYNTHESIS OF N-METHYL UROCANATES OF HYDROXYDERIVATIVES OF ISOCEMBROL F. A. Valeev,1 Sh. M. Salikhov,O. Yu. Krasnoslobodtseva,B. T. Sharipov L. V. Spirikhin, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-O-methylsartol A C21H36O2 ÏàËÆ¶È:76.1% Bulletin of the Chemical Society of Japan 1996 69 3543-3549 Ichthyotoxic Cembranoids from the Soft Coral, Sarcophyton sp. Tetsuo Iwagawa, Shun Nakamura, Hiroaki Okamura, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (1S,2E,4R,6R,7E,11E,13R)-2,7,11-cembratriene-4,6,13-triol C20H32O2 ÏàËÆ¶È:71.4% Acta Chemica Scandinavica 1993 47B 80-88 Tobacco Chemistry. 75. Two New Cembratrienetriols from Tobacco. Forsblom, Ingrid; Berg, Jan-Eric; Wahlberg, Inger Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (1S,2E,4R,6R,7E,11E,13R)-2,7,11-cembratriene-4-O-methyl-4,6,13-triol C21H36O3 ÏàËÆ¶È:71.4% Planta Medica 2011 77 467-476 Bioactive Natural, Biocatalytic, and Semisynthetic Tobacco Cembranoids Hany N. Baraka, Mohammad A. Khanfar, John C. Williams, Emad M. El-Giar, Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (1S,2E,4R,6R,7E,11E,13R)-6-acetoxy-2,7,11-cembratriene-4,13-diol ÏàËÆ¶È:70.8% Acta Chemica Scandinavica 1993 47B 80-88 Tobacco Chemistry. 75. Two New Cembratrienetriols from Tobacco. Forsblom, Ingrid; Berg, Jan-Eric; Wahlberg, Inger Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1E,5E,9R,10E,12S)-9-(Allyloxy)-12-isopropyl-1,5,9-trimethylcyclotetradeca-1,5,10-triene C23H38O ÏàËÆ¶È:69.5% Chemistry of Natural Compounds 2012 48 56-59 REACTION OF ISOCEMBROL AND ALCOHOLS ON CLAY O. I. Yarovaya,D. V. Korchagina,N. F. Salakhutdinov,and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Labda-7,11E,13Z-triene ÏàËÆ¶È:66.6% Phytochemistry 1992 31 615-620 Diterpenoids and cyclolanostanolides from Abies marocana Alejandro F. Barrero, Juan F. Sanchez, Enrique J. Alvarez-Manzaneda, Manuel Muñoz, Ali Haïdour Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (-)-(1S*,4R*,10R*)-1-hydroxy-4-methoxycembra-2E,7E,11Ztrien-20,10-olide C21H32O ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 2349-2355 Cembranolides from the Leaves of Croton gratissimus Moses K. Langat, Neil R. Crouch, Peter J. Smith, and Dulcie A. Mulholland Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 3-44 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1993 31 299-308 13C NMR data for labdane diterpenoids Alejandro F. Barrero and Joaquin Altarejos Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (1S,2E,4S,6R,7E,11E,13R)-6-acetoxy-2,7,11-cembratriene-4,13-diol ÏàËÆ¶È:63.6% Acta Chemica Scandinavica 1993 47B 80-88 Tobacco Chemistry. 75. Two New Cembratrienetriols from Tobacco. Forsblom, Ingrid; Berg, Jan-Eric; Wahlberg, Inger Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 15 C20H34O3 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1983 31 4409-4416 Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2) TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (15R)-isopimar-7-en-15,16-diol C20H34O2 ÏàËÆ¶È:61.9% Phytochemistry 1999 51 83-90 Diterpenes from the marine mangrove Bruguiera gymnorhiza Chitti Subrahmanyam, Battula Venkateswara Raoa, Robert S. Wardb, Michael B. Hursthousec, David E. Hibbs Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 14¦Á,16-oxido-ent-isopimar-7-en-15-one ÏàËÆ¶È:61.9% 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 15 . 7¦Á,11-dihydroxy-12-methoxy-8,11,13-abietatriene C21H32O3 ÏàËÆ¶È:61.9% Phytochemistry 1996 41 735-738 Antimicrobial abietane diterpenoids from Plectranthus elegans Joanne E. Dellar, Michael D. Cole, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . iso-odolide C20H28O2 ÏàËÆ¶È:61.9% Phytochemistry 1995 39 1399-1402 Diterpenoid lactones from the roots of Gynocardia odorata Bhim P. Pradhan, Satyajit Chakraborty, Rajat K. Ghosh, Animesh Roy Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S,2E,4S,6R,7E,11E,13R)-2,7,11-cembratriene-4,6,13-triol C20H34O3 ÏàËÆ¶È:61.9% Acta Chemica Scandinavica 1993 47B 683-688 Tobacco Chemistry. 76. Biotransformations of Tobacco Isoprenoids using Plant Cell Cultures of Tripterygium Wilfordii. Arnarp, Jan; Chu, W. L. Alexis; Enzell, Curt R.; Hewitt, Gary M.; Kutney, James P.; Li, Kai; MIlanova, Radka K.; Nakata, Hiroyuki; Nasiri, Ahmad; Okada, Yoshito Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1S,2E,4S,6R,7E,11E,13R)-2,7,11-cembratriene-4,6,13-triol ÏàËÆ¶È:61.9% Acta Chemica Scandinavica 1993 47B 80-88 Tobacco Chemistry. 75. Two New Cembratrienetriols from Tobacco. Forsblom, Ingrid; Berg, Jan-Eric; Wahlberg, Inger Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 4-O-methylsartone B C21H34O2 ÏàËÆ¶È:61.9% Bulletin of the Chemical Society of Japan 1996 69 3543-3549 Ichthyotoxic Cembranoids from the Soft Coral, Sarcophyton sp. Tetsuo Iwagawa, Shun Nakamura, Hiroaki Okamura, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (-)-(1R*,4R*,10R*)-4-methoxycembra-2E,7E,11Z-trien-20,10-olide C21H32O3 ÏàËÆ¶È:61.9% Journal of Natural Products 2011 74 2349-2355 Cembranolides from the Leaves of Croton gratissimus Moses K. Langat, Neil R. Crouch, Peter J. Smith, and Dulcie A. Mulholland Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 16,16-dimethyl-3-methoxy-D-homoestra-1,3,5(10),8,14-pentaen-17a¦Á-ol C22H28O2 ÏàËÆ¶È:61.9% Russian Journal of Organic Chemistry 2006 42 1675-1682 New analogs of D-homoequilenine with substituents in the D ring I. A. Gluzdikov, M. S. Egorov, S. I. Selivanov, G. L. Starova and A. G. Shavva Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (1S,4R,13S)-cembra-2E,7E,11E-trien-4,13-diol C20H34O2 ÏàËÆ¶È:61.9% Tetrahedron Letters 2013 54 989-992 Bioactive cembranoids from the Red Sea soft coral Sarcophyton glaucum Rania F. Abou El-Ezz, Safwat A. Ahmed, Mohamed M. Radwan, Nahla A. Ayoub, Manal S. Afifi,Samir A. Ross, Pawel T. Szymanski, Hesham Fahmy, Sherief I. Khalifa Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 138 ÏàËÆ¶È:61.9% 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 24 . (1S,2E,4R,7Z,11E)-2,7,11-cembratriene-4-O-methyl-4-ol-6-one C21H34O2 ÏàËÆ¶È:61.9% Planta Medica 2011 77 467-476 Bioactive Natural, Biocatalytic, and Semisynthetic Tobacco Cembranoids Hany N. Baraka, Mohammad A. Khanfar, John C. Williams, Emad M. El-Giar, Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 17-acetoxylabda-7,12(E),14-triene C22H34O2 ÏàËÆ¶È:59.0% Planta Medica 2003 69 167-170 Cytotoxic Activity of Natural Labdanes and their Semi-Synthetic Modified Derivatives from Croton oblongifolius Damrong Sommit,Amorn Petsom,Tsutomu Ishikawa,Sophon Roengsumran Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (1S,4S,SR)-4,5-dimethoxyeembra-2E,7E,11E-triene ÏàËÆ¶È:59.0% Chemistry of Natural Compounds 1994 30 595-598 CYCLIZATION OF CEMBRANE DITERPENOIDS VII. EXPERIMENTAL CONFIRMATION OF THE SCHEME OF ACID-CATALYZED CYCLIZATION OF 5¦Â-ACETOXYISOCEMBROL A. V. Shpatov, M. M. Shakirov,and V. A. Raldugin Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . dehydrootostegin B ÏàËÆ¶È:59.0% Phytochemistry 2000 54 771-775 Labdane diterpenes from Otostegia fruticosa Nawal M. Al-Musayeib, Fawkeya A. Abbas, M. Shamim Ahmad, Jaber S. Mossa, Farouk S. El-Feraly Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 6-O-Acetylaustroinulin C22H34O3 ÏàËÆ¶È:59.0% Canadian Journal of Chemistry 2006 84 1593-1602 Absolute configuration assignments by experimental and theoretical approaches of ent-labdane- and cis-ent-clerodane-type diterpenes isolated from Croton glabellus1 Abraham Garc¨ªa, Teresa Ram¨ªrez-Apan, J. Antonio Cogordan, and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . kalihinol S C22H35N2O3SCl ÏàËÆ¶È:59.0% Tetrahedron 2012 68 2876-2883 Antifouling and cytotoxic constituents from the South China Sea sponge Acanthella cavernosa Ying Xu, Nan Li, Wei-Hua Jiao, Ru-Ping Wang, Ying Peng, Shu-Hua Qi, Shao-Jiang Song, Wan-Sheng Chen, Hou-Wen Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (-)-menthyl O-4-butylphenyl phenylphosphonate C26H37O3P ÏàËÆ¶È:59.0% Tetrahedron 2013 69 9373-9380 Systematic study for the stereochemistry of the Atherton¨CTodd reaction Original Research Article Biquan Xiong, Yongbo Zhou, Changqiu Zhao, Midori Goto, Shuang-Feng Yin, Li-Biao Han Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 6-O-acetyl-austroinulin C22H36O4 ÏàËÆ¶È:59.0% Food and Chemical Toxicology 2013 62 638-644 Anti-inflammatory effect of austroinulin and 6-O-acetyl-austroinulin from Stevia rebaudiana in lipopolysaccharide-stimulated RAW264.7 macrophages Byoung Ok Cho, Hyung Won Ryu, Yangkang So, Jung Keun Cho, Hyun Sim Woo, Chang Hyun Jin, Kwon Il Seo, Jong Chun Park, Il Yun Jeong Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 19-norergosta-1,3,5,7,9,14,22-heptaene ÏàËÆ¶È:57.6% Tetrahedron 2012 68 6485-6491 Oxidation with selenium dioxide: the first report of solvent-selective steroidal aromatization, efficient access to 4¦Â,7¦Á-dihydroxy steroids, and syntheses of natural diaromatic ergosterols Pranab Ghosh, Jayanta Das, Antara Sarkar, Seik Weng Ng, Edward R.T. Tiekink Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (1S,12S)-ent-1-Hydroxyverticilla-3E,7E-dien-18-al C20H32O2 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2008 56(8) 1184-1188 New ent-Verticillane Diterpenoids from the Japanese Liverwort Jackiella javanica Fumihiro NAGASHIMA,Kozue WAKAYAMA, Yuki IOKA, and Yoshinori ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . doianoterpene A C20H28O2 ÏàËÆ¶È:57.1% Phytochemistry 2004 65 2071-2076 Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae) Naonobu Tanaka, Nobuyuki Ooba, Hongquan Duan, Yoshihisa Takaishi,Yuka Nakanishi, Kenneth Bastow, Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (1R,3E,7E,11R,12Z)-(+)-verticilla-3,7,12-triene ÏàËÆ¶È:57.1% Journal of Natural Products 2005 68 1598-1602 Verticillane Derivatives from Bursera suntui and Bursera kerberi Juan D. Hernndez-Hernndez, Luisa U. Romn-Marn, Carlos M. Cerda-Garca-Rojas, and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . ent-labda-8(17),12Z,14-trien-2r-ol C20H32O ÏàËÆ¶È:57.1% Journal of Natural Products 2003 66 491-496 Labdane and Kaurane Diterpenoids from Plectranthus fruticosus Cristina Gaspar-Marques, M. Ftima Simes, Aida Duarte, and Benjamn Rodrguez Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 13¦Á-hydroxy-14¦Á,16-epoxy-ent-abieta-7-en-3-one C20H30O3 ÏàËÆ¶È:57.1% Planta Medica 2009 75 641-646 ent-Abietane and ent-Kaurane Diterpenoids from the Roots of Suregada glomerulata Su-li He, Ren-yi Yan, Li Zuo, Ruo-yun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . isopimara-7,15-dien ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1982 30 3912-3921 Studies on the Constituents of the Crude Drug "Fritillariae Bulbus." III. On the Diterpenoid Constituents of Fresh Bulbs of Fritillaria thunbergii MIQ. JUNICHI KITAJIMA,TETSUYA KOMORI and TOSHIO KAWASAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . Methoxy-ent-8(14)-pimarenely-15-one C20H32O2 ÏàËÆ¶È:57.1% Molecules 2008 13 212-219 Antifouling Metabolites from the Mangrove Plant Ceriops tagal Jun D. Chen, Dan Q. Feng, Zhi W. Yang, Zhan C. Wang, Yan Qiu and Yi M. Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (1R,3E,7E,9S,11S,12Z)-9-hydroxy-dolabella-3,7,12-triene C20H32O ÏàËÆ¶È:57.1% Natural Product Research 2007 21 897-902 A new dolabellane diterpenoid from the Hainan soft coral Spongodes sp. Xiao-Hong Yan; Rui Jia; Xu Shen; Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 14¦Á-hydroxyisopimara-7,15-diene ÏàËÆ¶È:57.1% Phytochemistry 1997 45 387-390 Parryin, a diterpene with a tricyclic 6-7-5-ring system from Salvia parryi Elsa M. Guajardo Touche, Elda G¨®mez Loprz, Alfredo P. Reyes, Humberto S¨¢nchez, Friedrich Honecker, Hans Achenbach Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound ÏàËÆ¶È:57.1% Journal of Natural Products 1992 Vol 55 744 Labdane Diterpenes from Calceolaria densifolia Juan A. Garbarino, Aurora Molinari Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . Labda-7,12Z,14-triene C20H34 ÏàËÆ¶È:57.1% Phytochemistry 1992 31 615-620 Diterpenoids and cyclolanostanolides from Abies marocana Alejandro F. Barrero, Juan F. Sanchez, Enrique J. Alvarez-Manzaneda, Manuel Muñoz, Ali Haïdour Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Labda-8(17),12Z,14-triene ÏàËÆ¶È:57.1% Phytochemistry 1992 31 615-620 Diterpenoids and cyclolanostanolides from Abies marocana Alejandro F. Barrero, Juan F. Sanchez, Enrique J. Alvarez-Manzaneda, Manuel Muñoz, Ali Haïdour Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 9-(15,16-dihydro-15-methyl-enegeranyl)-p-cymene C21H32 ÏàËÆ¶È:57.1% Phytochemistry 1992 31 1727-1730 Homoditerpenes from the essential oil of Tanacetum annuum Alejandro F. Barrero, Juan F. S¨¢nchez, Joaqu¨ªn Altarejos, Maria J. Zafra Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . isopimaradiene ÏàËÆ¶È:57.1% Phytochemistry 1989 28 1675-1679 Diterpenoids of the wood of Agathis vitiensis Richard C. Cambie,Jan M. Coddington,Martin J. Stone,Nobutoshi Tanaka,Yong Hua Li,Sayuti Arigayo Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . sandaracopimaradiene C20H30O3 ÏàËÆ¶È:57.1% Magnetic Resonance in Chemistry 2004 42 893-897 Structural determination of novel terpenes from Buddleia lindleyana Jianghai Lu, Guangzhong Tu, Yuying Zhao, Yang Lv, Li Ying Liu and Yunshan Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . austroinulin C20H34O3 ÏàËÆ¶È:57.1% Phytochemistry 1980 19 153-155 Neue phloroglucin-derivate aus Helichrysum-arten Ferdinand Bohlmann, Christa Zdero Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 6-O-acetyl-austroinulin C22H36O4 ÏàËÆ¶È:57.1% Phytochemistry 1980 19 153-155 Neue phloroglucin-derivate aus Helichrysum-arten Ferdinand Bohlmann, Christa Zdero Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . compound 3 ÏàËÆ¶È:57.1% Phytochemistry 1982 21 395-397 Two labdane diterpenoids from Nicotiana raimondii Masana Noma, Fumiyo Suzuki, Kenji Gamou, Nobumaro Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . cis-abienol ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2010 46 298-300 Chemical constituents from Inula cappa Zhi-Jun Wu, Lei Shan, Min Lu, Yun-Heng Shen and Jian Tang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . Totata-8,11,13-trien-6¦Á,7¦Á,13-triol C20H30O3 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2000 8 1663-1675 The synthesis and antibacterial activity of totarol derivatives. part 3: modification of ring-B Gary B Evans, Richard H Furneaux, Graeme J Gainsford, Michael P Murphy Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . compound 1a C20H32O2 ÏàËÆ¶È:57.1% Tetrahedron 2012 68 819-829 Potential anti-inflammatory diterpenes from Premna obtusifolia Abdul-Wahab Salae, Apinya Rodjun, Chatchanok Karalai, Chanita Ponglimanont, Suchada Chantrapromma, Akkharawit Kanjana-Opas, Supinya Tewtrakul, Hoong-Kun Fun Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . compound 12 ÏàËÆ¶È:57.1% Acta Chemica Scandinavica 1988 42B 708-716 Tobacco Chemistry. 69. Five New Labdanic Compounds from Tobacco. Wahlberg, Inger; Eklund, Ann-Marie; Nordfors, Kerstin; Vogt, Carmen; Enzell, Curt R.; Berg, Jan-Eric Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 4-O-methylsarcotol C21H36O3 ÏàËÆ¶È:57.1% Bulletin of the Chemical Society of Japan 1996 69 3543-3549 Ichthyotoxic Cembranoids from the Soft Coral, Sarcophyton sp. Tetsuo Iwagawa, Shun Nakamura, Hiroaki Okamura, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . (3aR,4aS,8aR,9aR,E)-8a-methyl-5-methylidene-3-(4-chlorobenzylidene)decahydronaphtho[2,3-b]-furan-2(3H)-one C21H23O2Cl ÏàËÆ¶È:57.1% Russian Journal of Organic Chemistry 2010 46 1719-1734 Synthetic transformations of methylenelactones of eudesmanic type. Behavior of isoalantolactone under the conitions of heck reaction A. V. Belovodskii, E. E. Shults, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-27 14:20:43













»Ø¸´´ËÂ¥