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ÇóÖúÈý¸ö΢Æ×²éѯ ÒÑÓÐ1È˲ÎÓë
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Hsb-13 13C NMR (126 MHz,CDCl3) ¦Ä 16.37,23.59,24.41,25.73,29.83,30.77,34.51,35.36,40.21,40.73,46.53,66.79,68.88,75.11 Hsb-14 13C NMR (126 MHz,CDCl3) ¦Ä 20.65,29.83,55.45,56.41,56.56,97.08,106.01,108.95,117.18,127.6,136.68,138.57,156.86,157.53,157.77 Hsb-15 13C NMR (126 MHz,CDCl3) ¦Ä 13.71,14.15,18.51,18.64,19.1,20.51,22.72,29.21,29.38,29.72,30.6,31.8,31.95,44.3,47.47,55.39,56.31,56.44,64.69,76.78,77.04,77.29,96.97,106.48,108.31,114.87,116.11,116.51,117.82,120.29,128.21,131.84,136.67,136.88,153.67,156.6,157.29,157.6 |
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yuhaiqian: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-16 14:32:21
yuhaiqian: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-16 14:32:21
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²éѯ½á¹û£º¹²²éµ½657¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . dendrantheinoside A aglycone C13H24O3 ÏàËÆ¶È:71.4% Planta Medica 1992 58 373-375 Structural Elucidation of endranthemosides A and B:Two New f3-Ionone Glucosides from Dendranthema shiwogiku Hideaki Otsuka, Yasuyuki Takeda,Kazuo Yamasaki, and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . aglucone of dendranthemoside A ÏàËÆ¶È:71.4% Phytochemistry 1994 35 1331-1334 Alangionosides A and B, ionol glycosides from leaves of Alangium premnifolium Hideaki Otsuka, Kenji Kamada, Choei Ogimi, Eiji Hirata, Anki Takushi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3S,5R,6S,9R)-3,6-dihydro-5,6-dihydro-¦Â-ionol ÏàËÆ¶È:71.4% Natural Product Research and Development 2001 13(4) 5-7 STUDY ON THE CHEMICAL CONSTITUENTS OF MEZZETTIOPSIS CREAGHII RIDL. CHEN Bin; YANG Juan; LI Bo gang; ZHANG Guo lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Aglycone of crotonionoside C C13H24O3 ÏàËÆ¶È:71.4% Phytochemistry 2011 72 147-153 Crotonionosides A¨CG: Megastigmane glycosides from leaves of Croton cascarilloides Räuschel Susumu Kawakami, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1S,4S,6S)-1-(3-Hydroxy-but-1E-enyl)-2,2,6-trimethyl-cyclohexane-1,4-diol or (3S,5S,6S,9R)-3,6-Dihydroxy-5,6-dihydro-b-ionol ÏàËÆ¶È:71.4% Journal of the Brazilian Chemical Society 2009 20 1921-1924 Megastimanes and Ergostane Type Steroid from Leaves Cratylia mollis (Leguminosae) Luciano S. Lima, Marcos V. B. Lima, Juceni P. David, Ana M. Giulietti, Luciano P. de Queiroz and Jorge M. David Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9¦Â-bromo-4,8,11,11-tetramethylbicyclo[6.3.0]undecen-4-ene C15H25Br ÏàËÆ¶È:66.6% Journal of Natural Products 1994 Vol 57 738 Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (8S,9R)-isocaryolan-9-ol ÏàËÆ¶È:66.6% Journal of Natural Products 2013 76 1016-1024 Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure¨CActivity Relationships of Isocaryolane Derivatives Jociani Ascari, Maria Am¨¦lia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, Antonio J. Mac¨ªas-S¨¢nchez, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one C14H21OBr ÏàËÆ¶È:64.2% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (3S,5R,6S,9R)-3,6-dihydroxy-5,6-dihydro-¦Â-ionol C13H2403 ÏàËÆ¶È:64.2% Journal of Natural Products 1996 59 69-72 Absolute Structures of Two New C13-Norisoprenoids from Apollonias barbujana Cirilo Perez and Juan Trujillo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-(1',6'-Epoxy-2',2',6'-trimethyl-cyclohexyl)propionsaremethylester C13H22O3 ÏàËÆ¶È:64.2% Helvetica Chimica Acta 1980 63 1833-1855 Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität Alex Peter Alder, Hans Richard Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 9-epi-Kobusone C14H22O2 ÏàËÆ¶È:64.2% Phytochemistry 1994 35 1489-1494 Confirmation of structure and absolute stereochemistry of 9-epi-¦Â-caryophyllene from Dacrydium cupressinum Simon F.R. Hinkley, Nigel B. Perry, Rex T. Weavers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 7-megastigmene-3,6,9-triol ÏàËÆ¶È:64.2% Natural Product Research and Development 2002 14(5) 26-28 FLAVONOIDS FROM KNEMA GLOBULARIA MEI Wen li; NI Wei; HUA Yan; CHEN Chang xiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,2R)-2-chlorocyclopropanecarboxylic acid (1S,2R,5S)-5-isopropyl-2-methylcyclohexyl ester C14H23O2Cl ÏàËÆ¶È:64.2% Journal of the American Chemical Society 2002 124 10396-10415 Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues Barry M. Trost, Janet L. Gunzner, Olivier Dirat, and Young H. Rhee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Dihydroedulan C13H22O ÏàËÆ¶È:64.2% European Journal of Organic Chemistry 1989 1989 1195-1201 Epoxytetrahydroedulan, a New Terpenoid from the Hairpencils of Euploea (Lep.: Danainae) Butterflies Wittko Francke, Stefan Schulz, Volker Sinnwell, Wilfried A. König and Yves Roisin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (1S,2S)-Di-(-)-menthyl Cyclohex-4-ene-1,2-dicarboxylate ÏàËÆ¶È:64.2% Journal of Medicinal Chemistry 1989 32 197-202 Synthesis and biological evaluation of a monocyclic, fully functional analog of compactin Clayton H. Heathcock, Brian R. Davis, Cheri R. Hadley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Wilsonol E (3S,4S,5S,6S,9R) C13H26O3 ÏàËÆ¶È:64.2% Journal of Natural Products 2013 76 1303-1312 Wilsonols A¨CL, Megastigmane Sesquiterpenoids from the Leaves of Cinnamomum wilsonii Penghua Shu, Xialan Wei, Yongbo Xue, Weijie Li, Jinwen Zhang, Ming Xiang, Mengke Zhang, Zengwei Luo, Yan Li, Guangmin Yao, and Yonghui Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Wilsonol F C13H26O3 ÏàËÆ¶È:64.2% Journal of Natural Products 2013 76 1303-1312 Wilsonols A¨CL, Megastigmane Sesquiterpenoids from the Leaves of Cinnamomum wilsonii Penghua Shu, Xialan Wei, Yongbo Xue, Weijie Li, Jinwen Zhang, Ming Xiang, Mengke Zhang, Zengwei Luo, Yan Li, Guangmin Yao, and Yonghui Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 1,10-Epoxylepidozenol ÏàËÆ¶È:64.2% The Journal of Organic Chemistry 1990 55 3677-3679 Cytotoxic hydroperoxylepidozenes from the actinia Anthopleura pacifica Uchida Guo Chi Zheng, Akio Ichikawa, Midori O. Ishitsuka, Takenori Kusumi, Hiroshi Yamamoto, Hiroshi Kakisawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . isothiocyanate ÏàËÆ¶È:62.5% Experientia 1986 42 625-627 Minor nitrogenous sesquiterpenes from the marine spongeAxinella cannabina. A hypothesis for the biogenesis of the spiro-axane skeleton P. Ciminiello, E. Fattorusso, S. Magno and L. Mayol Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 8 ÏàËÆ¶È:62.5% Australian Journal of Chemistry 1988 41 979-983 New Isothiocyanate Sesquiterpenes From the Australian Marine Sponge Acanthella pulcherrima RJ Capon and JK Macleod Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-12-16 11:44:59
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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²éѯ½á¹û£º¹²²éµ½657¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . dendrantheinoside A aglycone C13H24O3 ÏàËÆ¶È:71.4% Planta Medica 1992 58 373-375 Structural Elucidation of endranthemosides A and B:Two New f3-Ionone Glucosides from Dendranthema shiwogiku Hideaki Otsuka, Yasuyuki Takeda,Kazuo Yamasaki, and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . aglucone of dendranthemoside A ÏàËÆ¶È:71.4% Phytochemistry 1994 35 1331-1334 Alangionosides A and B, ionol glycosides from leaves of Alangium premnifolium Hideaki Otsuka, Kenji Kamada, Choei Ogimi, Eiji Hirata, Anki Takushi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3S,5R,6S,9R)-3,6-dihydro-5,6-dihydro-¦Â-ionol ÏàËÆ¶È:71.4% Natural Product Research and Development 2001 13(4) 5-7 STUDY ON THE CHEMICAL CONSTITUENTS OF MEZZETTIOPSIS CREAGHII RIDL. CHEN Bin; YANG Juan; LI Bo gang; ZHANG Guo lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Aglycone of crotonionoside C C13H24O3 ÏàËÆ¶È:71.4% Phytochemistry 2011 72 147-153 Crotonionosides A¨CG: Megastigmane glycosides from leaves of Croton cascarilloides Räuschel Susumu Kawakami, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1S,4S,6S)-1-(3-Hydroxy-but-1E-enyl)-2,2,6-trimethyl-cyclohexane-1,4-diol or (3S,5S,6S,9R)-3,6-Dihydroxy-5,6-dihydro-b-ionol ÏàËÆ¶È:71.4% Journal of the Brazilian Chemical Society 2009 20 1921-1924 Megastimanes and Ergostane Type Steroid from Leaves Cratylia mollis (Leguminosae) Luciano S. Lima, Marcos V. B. Lima, Juceni P. David, Ana M. Giulietti, Luciano P. de Queiroz and Jorge M. David Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9¦Â-bromo-4,8,11,11-tetramethylbicyclo[6.3.0]undecen-4-ene C15H25Br ÏàËÆ¶È:66.6% Journal of Natural Products 1994 Vol 57 738 Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (8S,9R)-isocaryolan-9-ol ÏàËÆ¶È:66.6% Journal of Natural Products 2013 76 1016-1024 Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure¨CActivity Relationships of Isocaryolane Derivatives Jociani Ascari, Maria Am¨¦lia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, Antonio J. Mac¨ªas-S¨¢nchez, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one C14H21OBr ÏàËÆ¶È:64.2% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (3S,5R,6S,9R)-3,6-dihydroxy-5,6-dihydro-¦Â-ionol C13H2403 ÏàËÆ¶È:64.2% Journal of Natural Products 1996 59 69-72 Absolute Structures of Two New C13-Norisoprenoids from Apollonias barbujana Cirilo Perez and Juan Trujillo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-(1',6'-Epoxy-2',2',6'-trimethyl-cyclohexyl)propionsaremethylester C13H22O3 ÏàËÆ¶È:64.2% Helvetica Chimica Acta 1980 63 1833-1855 Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität Alex Peter Alder, Hans Richard Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 9-epi-Kobusone C14H22O2 ÏàËÆ¶È:64.2% Phytochemistry 1994 35 1489-1494 Confirmation of structure and absolute stereochemistry of 9-epi-¦Â-caryophyllene from Dacrydium cupressinum Simon F.R. Hinkley, Nigel B. Perry, Rex T. Weavers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 7-megastigmene-3,6,9-triol ÏàËÆ¶È:64.2% Natural Product Research and Development 2002 14(5) 26-28 FLAVONOIDS FROM KNEMA GLOBULARIA MEI Wen li; NI Wei; HUA Yan; CHEN Chang xiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,2R)-2-chlorocyclopropanecarboxylic acid (1S,2R,5S)-5-isopropyl-2-methylcyclohexyl ester C14H23O2Cl ÏàËÆ¶È:64.2% Journal of the American Chemical Society 2002 124 10396-10415 Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues Barry M. Trost, Janet L. Gunzner, Olivier Dirat, and Young H. Rhee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Dihydroedulan C13H22O ÏàËÆ¶È:64.2% European Journal of Organic Chemistry 1989 1989 1195-1201 Epoxytetrahydroedulan, a New Terpenoid from the Hairpencils of Euploea (Lep.: Danainae) Butterflies Wittko Francke, Stefan Schulz, Volker Sinnwell, Wilfried A. König and Yves Roisin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (1S,2S)-Di-(-)-menthyl Cyclohex-4-ene-1,2-dicarboxylate ÏàËÆ¶È:64.2% Journal of Medicinal Chemistry 1989 32 197-202 Synthesis and biological evaluation of a monocyclic, fully functional analog of compactin Clayton H. Heathcock, Brian R. Davis, Cheri R. Hadley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Wilsonol E (3S,4S,5S,6S,9R) C13H26O3 ÏàËÆ¶È:64.2% Journal of Natural Products 2013 76 1303-1312 Wilsonols A¨CL, Megastigmane Sesquiterpenoids from the Leaves of Cinnamomum wilsonii Penghua Shu, Xialan Wei, Yongbo Xue, Weijie Li, Jinwen Zhang, Ming Xiang, Mengke Zhang, Zengwei Luo, Yan Li, Guangmin Yao, and Yonghui Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Wilsonol F C13H26O3 ÏàËÆ¶È:64.2% Journal of Natural Products 2013 76 1303-1312 Wilsonols A¨CL, Megastigmane Sesquiterpenoids from the Leaves of Cinnamomum wilsonii Penghua Shu, Xialan Wei, Yongbo Xue, Weijie Li, Jinwen Zhang, Ming Xiang, Mengke Zhang, Zengwei Luo, Yan Li, Guangmin Yao, and Yonghui Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 1,10-Epoxylepidozenol ÏàËÆ¶È:64.2% The Journal of Organic Chemistry 1990 55 3677-3679 Cytotoxic hydroperoxylepidozenes from the actinia Anthopleura pacifica Uchida Guo Chi Zheng, Akio Ichikawa, Midori O. Ishitsuka, Takenori Kusumi, Hiroshi Yamamoto, Hiroshi Kakisawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . isothiocyanate ÏàËÆ¶È:62.5% Experientia 1986 42 625-627 Minor nitrogenous sesquiterpenes from the marine spongeAxinella cannabina. A hypothesis for the biogenesis of the spiro-axane skeleton P. Ciminiello, E. Fattorusso, S. Magno and L. Mayol Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 8 ÏàËÆ¶È:62.5% Australian Journal of Chemistry 1988 41 979-983 New Isothiocyanate Sesquiterpenes From the Australian Marine Sponge Acanthella pulcherrima RJ Capon and JK Macleod Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-16 11:44:41
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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²éѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Lyngbyastatin 8 C47H64N8O12 ÏàËÆ¶È:51.2% Marine drugs 2009 7 528-538 Lyngbyastatins 8¨C10,Elastase Inhibitors with Cyclic Depsipeptide Scaffolds Isolated from the Marine Cyanobacterium Lyngbya semiplena Jason C. Kwan,Kanchan Taori,Valerie J. Paul and Hendrik Luesch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . lyngbyastatin 5 C53H68N8O15 ÏàËÆ¶È:51.2% Journal of Natural Products 2007 70 1593-1600 Lyngbyastatins 5¨C7, Potent Elastase Inhibitors from Floridian Marine Cyanobacteria, Lyngbya spp. Kanchan Taori,Susan Matthew, James R. Rocca, Valerie J. Paul, and Hendrik Luesch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cyanostatin A C38H57N5O9 ÏàËÆ¶È:50% Phytochemistry 2005 66 543-548 Leucine aminopeptidase M inhibitors, cyanostatin A and B,isolated from cyanobacterial water blooms in Scotland Tomoharu Sano, Hiroo Takagi, Louise F. Morrison, James S. Metcalf,Geoffrey A. Codd, Kunimitsu Kaya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 21 C53H84N10O10 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 9405-9409 Total synthesis of (¡À)-martinelline Chengfeng Xia, Linshen Heng, Dawei Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . tetrahydropenitrem A C37H48ClNO6 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1983 1847-1856 Tremorgenic mycotoxins from Penicillium crustosum: isolation of penitrems A¨CF and the structure elucidation and absolute configuration of penitrem A Amelia E. de Jesus, Pieter S. Steyn, Fanie R. van Heerden, Robert Vleggaar, Philippus L. Wessels and William E. Hull Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 26 C36H43NO6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 6734-6741 Fluorescent schweinfurthin B and F analogs with anti-proliferative activity Joseph J. Topczewski, Craig H. Kuder, Jeffrey D. Neighbors, Raymond J. Hohl, David F. Wiemer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 54 C36H48O4S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 7570-7581 Relevance of the C-5 position to schweinfurthin induced cytotoxicity Joseph J. Topczewski, Michael P. Callahan, John G. Kodet, Jery D. Inbarasu, Nolan R. Mente, John A. Beutler, David F. Wiemer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
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- Ìû×Ó: 4735
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5Â¥2013-12-16 11:45:54













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