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1 . 7-Carboxyl-8-carveol ÏàËÆ¶È:69.2% Natural Product Research and Development 2014 26 1207-1211 Chemical Constituents from the Fruits of Dipteronia dyeriana SHI Ya-na, LIU Da-hui, JIN Hang, YANG Yan, ZHAO Da-ke, WANG Yue-hu, LONG Chun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 29 C16H30O4 ÏàËÆ¶È:62.5% Heterocycles 2008 76 1313-1328 2, 6-Dimethyl-4-nitrobenzoic Anhydride (DMNBA): An Effective Coupling Reagent for the Synthesis of Carboxylic Esters and Lactones Isamu Shiina and Ryo Miyao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (5Z,9Z)-14-methyl-5,9-pentadecadienoic acid C16H28O2 ÏàËÆ¶È:61.5% Journal of Natural Products 1997 60 502-504 Identification of the Novel Antimicrobial Fatty Acid (5Z, 9Z)-14-Methyl-5, 9-pentadecadienoic Acid in Eunicea succinea N¨¦stor M. Carballeira, Elba D. Reyes, Anthony Sostre, Abimael D. Rodr¨ªguez, Jorge L. Rodr¨ªguez, and Fernando A. Gonz¨¢ lez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . »·Ê®ÈýÄÚõ¥ ÏàËÆ¶È:61.5% Chemical Journal of Chinese Universities 2007 28 897-899 A New Method for Synthesis of Mcrocyclic Lactones via Malania Olceifera Chum Oil LIU Xiong-M in, LI Wei-Guang, LI Piao-Ying, ZHOU Yong0Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 6,7,8,9,10,11,12,13-octahydro-5H-cycloundeca[d]pyrimidine C13H20N2 ÏàËÆ¶È:61.5% Heterocycles 2006 70 581-586 One-Step Syntesis of 4,5-Disubstituted Pyrimidines Using Commercially Available and Inexpensive Reagents Phil S. Baran,* Ryan A. Shenvi, and Steven A. Nguyen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N1-(3-aminopropyl)-N3-cyclopentadecylpropane-1,3-diamine C21H45N3 ÏàËÆ¶È:61.5% Journal of Medicinal Chemistry 2014 57 4023-4034 Synthesis and Biological Evaluation of Antimetastatic Agents Predicated upon Dihydromotuporamine C and Its Carbocyclic Derivatives Aaron Muth, Veethika Pandey, Navneet Kaur, Melissa Wason, Cheryl Baker, Xianlin Han, Teresa R. Johnson, Deborah A. Altomare, and Otto Phanstiel, IV Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4,5,6,7,8,9,10,11,12,13-Decahydro-2-[(2H3)methyl]-1H-cyclopenta[12]annulene ( ÏàËÆ¶È:60% Helvetica Chimica Acta 2009 92 1782-1799 Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl 2-(2-ethylidenecyclooctyl)-3-methoxypropionate C15H26O3 ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung B 2001 56 1227-1234 Facile Approach to ersatile Chiral Intermediates for Fused Cyclopentanoid Natural Products F. Zulfiqar and A. Malik Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1-ethylcyclotridec-1-ene C15H28 ÏàËÆ¶È:57.1% Russian Journal of Organic Chemistry 2010 46 807-811 RegioselectiveintermolecularcycloaluminationofcyclicallenesandethylenewithRnAlCl3−n,catalyzedbytitaniumandzirconiumcomplexes V. A. D¡¯yakonov, R. K. Timerkhanov and U. M. Dzhemilev Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-[(2-2H)ethyl](13-2H)cyclotridec-1-ene C15H26D2 ÏàËÆ¶È:57.1% Russian Journal of Organic Chemistry 2010 46 807-811 RegioselectiveintermolecularcycloaluminationofcyclicallenesandethylenewithRnAlCl3−n,catalyzedbytitaniumandzirconiumcomplexes V. A. D¡¯yakonov, R. K. Timerkhanov and U. M. Dzhemilev Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-[(1-methylamino)phenylmethyl]cyclooctane-1-thiol hydrochloride C16H25NS ÏàËÆ¶È:57.1% Tetrahedron 2012 68 9016-9022 Facile access to ¦Ã-aminothiols from 1,3-thiazines via a microwave-assisted three-component reaction Flavie Peudru, Remi Legay, Jean-François Lohier, Vincent Reboul, Mihaela Gulea Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1,3-bis-(6-carboxypentyl)-4-pentylimidazolium C20H34N2O4 ÏàËÆ¶È:57.1% Chemical Research in Toxicology 2003 16 232-241 Model Studies on the Modification of Proteins by Lipoxidation-Derived 2-Hydroxyaldehydes Zhongfa Liu and Lawrence M. Sayre Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . oxacyclopentadecan-2-one C14H26O2 ÏàËÆ¶È:57.1% Flavour and Fragrance Journal 2012 27 75-76 Isolation and identification of oxacyclopentadecan-2-one from the dried fruiting body of Dictyophora echinovolvata Zang, Zheng et Hu Mingquan Huang, Hongyu Tian, Baoguo Sun and Yuping Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . maninsigin C C16H28O2 ÏàËÆ¶È:56.2% Fitoterapia 2013 84 58-63 Bioactive phenolics and terpenoids from Manglietia insignis Shan-Zhai Shang, Ling-Mei Kong, Li-Ping Yang, Jing Jiang, Jin Huang, Hai-Bo Zhang, Yi-Ming Shi, Wei Zhao, Hong-Lin Li, Huai-Rong Luo, Yan Li, Wei-Lie Xiao, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-Chloro-3-Methylcyclopentadecan-1-one C16H29OCl ÏàËÆ¶È:56.2% Flavour and Fragrance Journal 2012 27 54-59 Expedient synthesis of (E)-3-methylcyclopentadec-2-en-1-one, an important precursor for (R)-(− musconesHisahiro Hagiwara, Teppei Adachi, Masaharu Doya, Takashi Hoshi and Toshio Suzuki Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 8 C18H28O4 ÏàËÆ¶È:55.5% Journal of Natural Products 2003 66 1318-1323 Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 6a C17H21N3O ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 1987 35 2646-2655 Highly Regioselective Synthesis of Trisubstituted Pyrrolidines by 1, 3-Cycloaddition NOBUYUKI IMAI and KAZUO ACHIWA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 7-acetoxy-p-menth-1-en-8-ol ÏàËÆ¶È:53.8% Biochemical Systematics and Ecology 1995 23 875-876 Grilactone and other Terpenoids from Anthriscus nitida Bernard Muckensturm, Fouzia Diyani, Jean-Pierre Reduron Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound Ia ÏàËÆ¶È:53.8% Acta Pharmaceutica Sinica 1992 27 752-757 NEW MONOTERPENOIDS FROM CYNANCHUM HANCOCKIANUM HX Lou; X Li; TR Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 7-hydroxyterpineol C10H16O ÏàËÆ¶È:53.8% Phytochemistry 1991 30 583-587 Sesquiterpene lactones and other constituents from Artemisia xerophytica R. X. Tan, J. Jakupovic, F. Bohlmann, Z. J. Jia, S. Huneck Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . bicyclo[2.2.2]octane(g) ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1976 59 2437-2442 13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . oleuropeic acid methylester ÏàËÆ¶È:53.8% Planta Medica 1994 60 467-469 Monoterpene Glucosides from Cunila spicata Manns, D.; Hartmann, R. Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 1,4-Dioxaspiro[4.15]icosane ÏàËÆ¶È:53.8% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . cis-(Z)-oxacyclotridec-10-en-2-one ÏàËÆ¶È:53.8% Phytochemistry 1989 28 3311-3315 (Z)-oxacyclotridec-10-en-2-one,an alfalfa weevil feeding deterrent from Medicago rugosa Robert P. Doss,Steven J. Gould,Kathleen J.R. Johnson,Robert A. Flath,Rodger L. Kohnert Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Compound 4a ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 2001 39 222-224 1H and 13C NMR spectral assignments for 3, 5-disubstituted tetrahydro-2H-1, 3, 5-thiadiazine-2-thione derivatives Dolores Molero, Rolando P¨¦rez, Roberto Martinez, Margarita Su¨¢rez, Hortensia Rodriguez, Nazario Mart¨ªn and Carlos Seoane Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 1 C14H21N2OPS ÏàËÆ¶È:53.8% Tetrahedron Letters 2004 45 3855-3859 Synthesis of chiral ortho-thio-substituted phenyl phosphonodiamidates via a P-S to P-C rearrangement Christelle Mauger, Michel Vazeux, Serge Masson Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 7 ÏàËÆ¶È:53.8% Tetrahedron Letters 1991 32 7001-7004 Structure and synthesis of a new butanolide from a marine actinomycete Charles Pathirana, Ryan Dwight, Paul R. Jensen, William Fenical, Antonio Delgado, Linda S. Brinen, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (Z)-3,7-dimethyl-6,7-isopropylidenedioxy-2-octenal C13H22O3 ÏàËÆ¶È:53.8% Russian Journal of Organic Chemistry 2002 38 1594-1605 Transformations of 6,7-Epoxy Derivatives of Citral and Citronellal in Various Acidic Media O. I. Yarovaya, O. V. Salomatina, D. V. Korchagina, M. P. Polovinka and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (3-methyl-3-butenyl)dicyclohexylphosphane sulfide C17H31PS ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2010 1562-1568 nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds Arnaud Perrier, Virginie Comte, Claude Moïse, Philippe Richard and Pierre Le Gendre Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (2-phenylethyl)dicyclohexylphosphane sulfide ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2010 1562-1568 nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds Arnaud Perrier, Virginie Comte, Claude Moïse, Philippe Richard and Pierre Le Gendre Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (4S)-7-bromo-p-methyl-1-en-8-ol ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1992 45 2077-2081 ¦Ä-Terpineol SD Bull and RM Carman Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . racemic p-menth-1-ene-7,8-diol C10H18O2 ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1993 46 441-447 7-Hydroxy- l,8-cineole and 7-Cineolic Acid. Two New Possum Urinary Metabolites SD Bull, RM Carman, FN Carrick and KD Klika Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . compound 11b C16H32O2Si ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1996 49 741-749 7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites RM Carman and AC Garner Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ¦Á-(1R,2R,4S)-1,2-epoxy-p-mentha-7,8-diol C16H32O3Si ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1996 49 741-749 7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites RM Carman and AC Garner Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 8-hydroxy-p-menth-1-en-7-al C10H16O2 ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1996 49 741-749 7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites RM Carman and AC Garner Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (+)-¦Á-terpineol ÏàËÆ¶È:53.8% Indian Journal of Chemistry Section B 1999 38B 515-517 Microbial oxidation of ¦Á-pinene to(+)-¦Á-terpineol by Candida tropicalis T Chatterjee, B K De & D K Bhattacharyya Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . oleuropeic acid ÏàËÆ¶È:53.8% Journal of Guangdong Phamaceutical University 2008 24 33-35 Chemical constituents of the extracts from Ledum palustre L.Var. Angustum E.Busch(¢ò) HUANG Ying, ZHANG De-zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . terpineol ÏàËÆ¶È:53.8% Chinese Journal of Natural Medicines 2013 11 264-268 Chemical constituents of Cinnamomum cebuense Consolacion Y. Ragasa, Dinah L. Espineli, Esperanza Maribel G. Agoo, Ramon S. del Fierro Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 2-azacycloundecanone C10H19NO ÏàËÆ¶È:53.8% The Journal of Organic Chemistry 2002 67 245-258 Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (E,Z)-oxacyclotetradec-11-en-2-one ÏàËÆ¶È:53.8% Tetrahedron 2013 69 7408-7415 Efficient, durable and reusable olefin metathesis catalysts with high affinity to silica gel Original Research Article Krzysztof Skowerski, Piotr Kasprzycki, Michał Bieniek, Tomasz K. Olszewski Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . ¦Á-terpineol ÏàËÆ¶È:53.8% Molecules 2013 18 10733-10746 Identification of Repellent and Insecticidal Constituents of the Essential Oil of Artemisia rupestris L. Aerial Parts against Liposcelis bostrychophila Badonnel Xin Chao Liu, Yin Ping Li, He Qin Li, Zhi Wei Deng, Ligang Zhou, Zhi Long Liu and Shu Shan Du Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound 49 ÏàËÆ¶È:53.8% Organic Magnetic Resonance 1975 7 426-432 13C-NMR-Spektren von Monoterpenen F. Bohlmann, R. Zeisberg and E. Klein Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 1-Cyclohexylidene-3-fluoro-2-oxaspiro[4.5]dec-3-ene C15H21FO ÏàËÆ¶È:53.8% Synthesis 2014 46 1493-1505 Nucleophilic 5-endo-trig Cyclization of 3,3-Difluoroallylic Metal Enolates and Enamides:Facile Synthesis of Ring-Fluorinated Dihydroheteroles Fujita, Takeshi; Ikeda, Masahiro; Hattori, Masahiro; Sakoda, Kotaro; Ichikawa, Junji Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . cis-1-amino-octahydro-quinolizin-4-one C9H16N2O ÏàËÆ¶È:53.8% Tetrahedron 2012 68 5547-5553 Reductive transformations of unsaturated azabicyclic nitrolactams Mih¨¢ly Viktor Pilipecz, Tam¨¢s R¨®bert Varga, P¨¢l Scheiber, Zolt¨¢n Mucsi, Am¨¦lie F¨¤vre-Mourgues, S¨¢ndor Boros, L¨¢szl¨® Bal¨¢zs, G¨¢bor T¨®th, P¨¦ter Nemes Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . p-Menth-1-en-8-ol ÏàËÆ¶È:53.8% Journal of Agricultural and Food Chemistry 2006 54 9079-9084 Odor-Active Alcohols from the Fungal Transformation of ¦Á-Farnesene Ulrich Krings, Björn Hardebusch, Dieter Albert, Ralf G. Berger, Mario Mar¨®stica, Jr., and Glaucia M. Pastore Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . 1-(1-methyl-1-isothiocyano-ethyl)-4-methyl-3-cyclohexene C11H16O ÏàËÆ¶È:53.8% Journal of the Brazilian Chemical Society 2001 12 661-666 Controlling Factors Determining the Selective HSCN Addition to Double Bonds and Their Application to the Synthesis of 7-Isothiocyano-7,8-¦Á-Dihydro-Bisabolene Cec¨ªlia M. de Oliveira, Cleuza C. da Silva, Carol H. Collins and Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 2-(4-Methylcyclohex-3-enyl)propan-2-ol ÏàËÆ¶È:53.8% Tetrahedron 2012 68 7414-7421 Amberlyst®-15: a reusable heterogeneous catalyst for the dehydration of tertiary alcohols Lu¨ªs M.T. Frija, Carlos A.M. Afonso Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 9-Methyl-(Z)-5-decenyl Acetate C13H24O2 ÏàËÆ¶È:53.8% Journal of Chemical Ecology 1991 17 103-122 Alkyl substitution in terminal chain of (Z)-5-decenyl acetate, a pheromone component of turnip moth,Agrotis segetum. Synthesis, single-sensillum recordings, and structure-activity relationships Stig Jönsson, Tommy Liljefors, Bill S. Hansson Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 11-Oxa-(Z)-5-dodecenyl Acetate C13H24O3 ÏàËÆ¶È:53.8% Journal of Chemical Ecology 1995 21 815-832 Alkyl ether and enol ether analogs of (Z)-5-decenyl acetate, a pheromone component of the turnip moth,Agrotis segetum: probing a proposed bioactive conformation for chain-elongated analogs Anna-Lena Gustavsson, Tommy Liljefors, Bill S. Hansson Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . terpineol C10H18O ÏàËÆ¶È:53.8% Chemistry and Industry of Forest Products 2014 34 71-76 Chemical Constituents of Ginkgo Biloba L.Leaves Lipids TAO Ranl, WANG Cheng-zhang.KONG Zhen-wul Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 6,6'-((6-(but-3-yn-1-ylamino)-1,3,5-triazine-2,4-diyl)bis(azanediyl))dihexanoic acid C19H30N6O4 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2014 22 6288-6296 Sequential and parallel dual labeling of nanoparticles using click chemistry Hong Zong, Sascha N. Goonewardena, Huai-Ning Chang, James B. Otis, James R. Baker Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . (1S,2R,5S,6R,7R)-N,2-Dimethyl-5-(1-methylethyl)bicyclo[4.1.0]heptane-7-carboxamide C13H23NO ÏàËÆ¶È:53.8% Chemistry & Biodiversity 2014 11 1782-1797 Synthesis and Sensory Studies of Umami-Active Scaffolds Michael Backes, Susanne Paetz, Tobias Vössing and Jakob Peter Ley Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . compound 5a C16H30O5S ÏàËÆ¶È:53.3% Chinese Chemical Letters 2008 19 403-405 Synthesis of macrocyclic lactones with methoxysulfonyl side chain Chuan Jin Hou, Xiao Mei Liang, Jing Ping Wu, Dao Quan Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . compound 1 C15H22O2 ÏàËÆ¶È:53.3% Phytochemistry 1998 47 301-302 A sesquiterpene class from Illicium dunnianum Lai-King Sy, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . lippifolian-1(6)-en-4¦Â-ol-5-one CI5H22O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1994 Vol 57 206 Minor Constituents of Lippia integrifolia Cesar A. N. Catal¨¢n, Marina E. P. de Lampasona, In¨¦s J. S. de Fenik, Carlos M. Cerda-Garc¨ªa-Rojas, Yolanda Mora-P¨¦rez, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . eleganthol C15H26O3 ÏàËÆ¶È:53.3% Phytochemistry 1993 32 1493-1497 Eleganthol, a sesquiterpene from Clitocybe elegans Alberto Arnone, Arturo Colombo, Gianluca Nasini, Stefano Valdo Meille Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . Methyl (1Z)-Cyclotridec-1-ene-1-carboxylate ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . rac-(6Z)-1-Oxaspiro[2.14]heptadec-6-ene ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . (6E)-1,4-Dioxaspiro[4.15]icos-6-ene ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . Cyclohexan-carbaldehyde ÏàËÆ¶È:53.3% Tetrahedron Letters 2001 42 6531-6534 Isochromans from 2-(3',4'-dihydroxy)phenylethanol Marcella Guiso, Carolina Marra, Claudia Cavarischia Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . compound 2 ÏàËÆ¶È:53.3% Tetrahedron 1986 42 2707-2716 13C NMR and 1H lanthanide induced shifts of naturally occurring alkamides with cyclic amide moieties -amides from achilleafalcata Otmar Hofer, Harald Greger, Wolfgang Robien, Andreas Werner Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . compound 21 C23H49N3 ÏàËÆ¶È:53.3% The Journal of Organic Chemistry 2002 67 245-258 Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . compound 9(n=10)ketone ÏàËÆ¶È:53.3% Canadian Journal of Chemistry 1977 55 3261-3267 13C chemical shifts in medium ring and macrocyclic ketolactones Jaswant R. Mahajan, Hugo C. Ara¨²jo Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . compound 9(n=10)oxime ÏàËÆ¶È:53.3% Canadian Journal of Chemistry 1977 55 3261-3267 13C chemical shifts in medium ring and macrocyclic ketolactones Jaswant R. Mahajan, Hugo C. Ara¨²jo Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . (Z)-3-(Cyclododec-1-en-1-yl)propanal ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2011 94 1216-1225 A Novel Synthesis of ¦Ã,¦Ä-Unsaturated Aldehydes from ¦Á-Formyl-¦Ã-lactones Roger L. Snowden*, Robert Brauchli, and Simon Linder Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . rel-(2R,8S,8aR)-2-(1,2,6,7,8,8a-Hexahydro-8,8a-dimethyl-2-naphthyl)-propan-2-ol ÏàËÆ¶È:53.3% Flavour and Fragrance Journal 1995 10 147-152 Agarwood oil (Aquilaria agallocha Roxb.) Its composition and eight new valencane-,eremophilane- and vetispirane- derivatives R. Näf, A. Velluz, R. Brauchli and W. Thommen Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . Trichodone A C15H26O3 ÏàËÆ¶È:53.3% 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 68 . (4¦Á,7¦Â,9¦Á)-Farfugane-4,9,11-triol C15H28O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2013 96 445-451 Six Novel Eudesmane-Like Sesquiterpenes from Illicium spathulatum Xu-Jun Dong and Shi-De Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . cyclonerodiol C15H28O3 ÏàËÆ¶È:53.3% Journal of Shenyang Pharmaceutical University 2013 30 342-345 Secondary metabolites from marine sponge-associated fungus Hansfordia sp. ZHAO Dan-qi, WU Ze-hong, LIU Dong, PEI Yue-hu, LIN Wen-han, BAI Jiao Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . isotripiperideine ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung C 1988 43 363-369 On the Role of ¡÷1-Piperideine and Tripiperideine in the Biosynthesis of Quinolizidine Alkaloids Ralf Perrey and Michael Wink Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . rac-1-Oxaspiro[2.15]octadec-7-ene ÏàËÆ¶È:52.9% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . N-[(2E,4E,8Z,)-tetradecatrienoyl]piperidine C19H31NO ÏàËÆ¶È:52.9% Journal of Agricultural and Food Chemistry 2005 53 1435-1439 Piperidinyl Amides with Insecticidal Activity from the Maritime Plant Otanthus maritimus Lito Christodoulopoulou, Maria Tsoukatou, Leto A. Tziveleka, Constantinos Vagias, Panos V. Petrakis, and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . eiseniaiodide B C18H29IO3 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 1318-1323 Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . cyclonerodiol oxide C15H29O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1984 32 4419-4425 Fungal Metabolites. II. Structural Elucidation of Minor Metabolites, Valinotricin, Cyclonerodiol Oxide, and Epicyclonerodiol Oxide, from Trichoderma polysporum TETSURO FUJITA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSUJI FUJIYAMA and TAKAHITO NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . 3-[(2H3)Methyl]cyclopentadecanone ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 1782-1799 Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . 5,16-Dioxo-1-azacyclohexadecane-2-carbonitrile C16H26N2O2 ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 2774-2782 Synthesis of 15-Cyano-12-oxopentadecano-15-lactone and 15-Cyano- 12-oxopentadecano-15-lactam Peng Wu, Xiao-Mei Liang, Jian-Jun Zhang, Yue-Mei Jia, Yan-Hong Dong, Jia-Xing Huang, Fu-Heng Chen, Dao-Quan Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . compound 2 C14H24O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2011 21 2456-2459 Biotransformation of natural compounds. Oxido-reduction of Sch-642305 by Aspergillus ochraceus ATCC 1009 Emilie Adelin, Claudine Servy, Sylvie Cortial, H¨¦l¨¨ne L¨¦vaique, Jean François Gallard,Marie-Th¨¦r¨¨se Martin, Pascal Retailleau, Boonsom Bussaban, Saisamorn Lumyong, Jamal Ouazzani Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . (4R,4aR,8aR)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol C14H24O ÏàËÆ¶È:50% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . (4R,4aR,8aR)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol C14H24O ÏàËÆ¶È:50% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . Hexyl-6-(2,5-dioxopyrrolidin-1-yl)hexanoate C16H27NO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 86-95 Investigation of substituted 6-aminohexanoates as skin penetration enhancers Katerina Brychtova, Lenka Dvorakova, Radka Opatrilova, Ivan Raich, Sandra Kacerova,Lukas Placek, Danuta S. Kalinowski, Des R. Richardson, Josef Jampilek Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . Methyl (1Z)-Cyclododec-1-ene-1-carboxylate ÏàËÆ¶È:50% |

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