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ÈܼÁ£ºÈ«²¿ ²éѯ½á¹û£º¹²²éµ½254¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Benzyl-(11-phenyl-undec-10-ynyl)-amine ÏàËÆ¶È:65% Archiv der Pharmazie 2007 340 154-158 Synthesis and Biological Evaluation of New Niphathesine Analogues J¨¹rgen Krauss, Christine Wetzel, Julia Thiel, Christine Neudert and Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3Z,6Z,9Z)-3,6,9-Docosatriene ÏàËÆ¶È:63.6% Journal of Agricultural and Food Chemistry 2007 55 6929-6932 Facile and Efficient Syntheses of (3Z,6Z,9Z)-3,6,9-Nonadecatriene and Homologues: Pheromone and Attractant Components of Lepidoptera Shifa Wang and Aijun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3Z,6Z,9Z)-3,6,9-Heneicosatriene ÏàËÆ¶È:61.9% Journal of Agricultural and Food Chemistry 2007 55 6929-6932 Facile and Efficient Syntheses of (3Z,6Z,9Z)-3,6,9-Nonadecatriene and Homologues: Pheromone and Attractant Components of Lepidoptera Shifa Wang and Aijun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (3Z,6Z,9Z)-3,6,9-tricosatriene ÏàËÆ¶È:60.8% Journal of Agricultural and Food Chemistry 2007 55 6929-6932 Facile and Efficient Syntheses of (3Z,6Z,9Z)-3,6,9-Nonadecatriene and Homologues: Pheromone and Attractant Components of Lepidoptera Shifa Wang and Aijun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-Benzyl-3-octylthiomethylbenzimidazolium chloride ÏàËÆ¶È:60% Archiv der Pharmazie 1997 330 253-258 Synthesis and Antimicrobial Activity of New 1-Benzylbenzimidazolium Chlorides Juliusz Pernak, Anita Arndt and Bogumil Brycki Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (Z,Z)-7,15-tetracosadiene-1,24-diol bis 3-hydroxypropanoate ester C24H46O2 ÏàËÆ¶È:60% Tetrahedron 2000 56 7633-7641 Bruchins¡ªMitogenic 3-(Hydroxypropanoyl) Esters of Long Chain Diols from Weevils of the Bruchidae James E Oliver, Robert P Doss, R.Thomas Williamson, John R Carney, E.David DeVilbiss Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-phenyl-4-(S)-[(4S,5S)-4-(tetradecyl)-1,3,2-dioxathiolane-2,2-dioxide-5-yl]-1,3-oxazoline C25H39NO5S ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 6685-6689 A Rapid and Efficient Synthesis of D-erythro-Sphingosine from D-ribo-Phytosphingosine Richard J. B. H. N. van den Berg, Hans van den Elst, Cornelius G. N. Korevaar, Johannes M. F. G. Aerts, Gijsbert A. van der Marel and Herman S. Overkleeft Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-phenyl-4-(S)-[(1S,2E)-1-hydroxyhexadec-2-enyl]-1,3-oxazoline C25H39NO2 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 6685-6689 A Rapid and Efficient Synthesis of D-erythro-Sphingosine from D-ribo-Phytosphingosine Richard J. B. H. N. van den Berg, Hans van den Elst, Cornelius G. N. Korevaar, Johannes M. F. G. Aerts, Gijsbert A. van der Marel and Herman S. Overkleeft Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . hexadecyl(phenyl)selane ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 1940-1946 Magnetically Separable and Reusable Copper Ferrite Nanoparticles for Cross-Coupling of Aryl Halides with Diphenyl Diselenide Kokkirala Swapna, Sabbavarapu Narayana Murthy and Yadavalli Venkata Durga Nageswar Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (3Z,6Z,9Z)-3,6,9-Eicosatriene ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 2007 55 6929-6932 Facile and Efficient Syntheses of (3Z,6Z,9Z)-3,6,9-Nonadecatriene and Homologues: Pheromone and Attractant Components of Lepidoptera Shifa Wang and Aijun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . sorgoleone-386 ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 2003 51 7589-7595 Chromatographic Separation and in Vitro Activity of Sorgoleone Congeners from the Roots of Sorghum bicolor Isabelle A. Kagan, Agnes M. Rimando, and Franck E. Dayan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-chloro-6,7,8,9,10,11,12,13,14,15-decahydro-16-phenylcyclododecaquinoline C25H28ClN ÏàËÆ¶È:59.0% Heterocycles 2008 75 947-954 Green Protocol for the Friedländer Synthesis: KAl(SO4)2¡¤12H2O-SiO2 (Alum- SiO2), a Highly Efficient Catalyst in the Synthesis of Quinolines Ali A. Mohammadi, Javad Azizian, Armin Hadadzahmatkesh, and Mohammad R. Asghariganjeh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 9k C34H36Br2S ÏàËÆ¶È:59.0% Tetrahedron 2013 69 1904-1911 Synthesis of an alkylthio-substituted dibenz[a,j]anthracene with improved solubility via the oxidative photocyclization of 1,3-distyrylbenzene derivatives Takuya Toyoshima, Satoshi Yoshida, Soichiro Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-[(9Z)-Octadec-9-enoyl]-5-phenylsemicarbazides ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2010 20 1933-1938 Synthesis, characterization, and in vitro antimicrobial activities of 5-alkenyl/hydroxyalkenyl-2-phenylamine-1,3,4-oxadiazoles and thiadiazoles Nida N. Farshori, Mudasir R. Banday, Anis Ahmad, Asad U. Khan, Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . mixture of (3E,5Z)-tetradeca-3,5,13-trien-2-amine and (3E,5E)-tetradeca-3,5,13-trien-2-amine C14H25N ÏàËÆ¶È:57.1% Australian Journal of Chemistry 1991 44 627-633 Cytotoxic and Antifungal C14 Amines From a New Zealand Ascidian: Major Lipid Components of Pseudodistoma novaezelandiae NB Perry, JW Blunt and MHG Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1',2'-dihydroxy-3-pentadeca-8,11-dienylbenzene ÏàËÆ¶È:57.1% Journal of Ethnopharmacology 2012 139 142-148 Catechol alkenyls from Semecarpus anacardium: Acetylcholinesterase inhibition and binding mode predictions H.R. Adhami, T. Linder, H. Kaehlig, D. Schuster, M. Zehl, L. Krenn Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (Z)-N-Benzyltetracos-15-enamide C31H53NO ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2013 21 5188-5197 Macamides and their synthetic analogs: Evaluation of in vitro FAAH inhibition Hui Wu, Charles J. Kelley, Alejandro Pino-Figueroa, Huyen D. Vu, Timothy J. Maher Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . gerronemin F C28H38O4 ÏàËÆ¶È:56.5% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . S-1-dodecyl 2-(N-benzylbenzamido)ethanethioate C28H39NO2S ÏàËÆ¶È:56.5% Heterocycles 2007 73 403-417 A Versatile Synthesis of ¦Á-Amino Acid Derivatives via the Ugi Four-Component Condensation with a Novel Convertible Isonitrile Kentaro Rikimaru, Arata Yanagisawa, Toshiyuki Kan, and Tohru Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . S-1-dodecyl 2-(N-phenylbenzamido)-3-methylbutanethioate C30H43NO2S ÏàËÆ¶È:56.5% Heterocycles 2007 73 403-417 A Versatile Synthesis of ¦Á-Amino Acid Derivatives via the Ugi Four-Component Condensation with a Novel Convertible Isonitrile Kentaro Rikimaru, Arata Yanagisawa, Toshiyuki Kan, and Tohru Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (S,Z)-1-benzoyloxynonadec-10-en-2-ol ÏàËÆ¶È:56.5% Tetrahedron 2012 68 2973-2983 Synthesis of (Z)-(2'R)-1-O-(2'-methoxynonadec-10'-enyl)-sn-glycerol, a new analog of bioactive ether lipids Ren¨¦ Pemha, Dieudonn¨¦ Emmanuel Pegnyemb, Paul Mosset Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3(R)-benzoyloxy-2(R)-methyl-6(R)-(11'-oxododecyl)-piperidine C25H39NO3 ÏàËÆ¶È:56% Planta Medica 2003 69 1054-1056 Cytotoxic Alkaloids from the Flowers of Senna spectabilis Lawan Sriphong,Uthai Sotanaphun, Siripan Limsirichaikul,Penpan Wetwitayaklung, Chaiyo Chaichantipyuth,Sunibhond Pummangura Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . gerronemin B C24H32O4 ÏàËÆ¶È:55% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . gerronemin D C26H36O4 ÏàËÆ¶È:55% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-(Undec-10-enoyl)-4-benzoyl-thiosemicarbazide C19H27N3O2S ÏàËÆ¶È:55% Chinese Chemical Letters 2008 19 1427-1430 Synthesis and evaluation of in vitro antibacterial activity of novel 2,5-disubstituted-1£¬3£¬4-thiadiazoles from fatty acids Mudasir R£®Banday,Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2-Benzamido-5-(heptadec-8-enyl)-1 ,3,4-thiadiazole C26H39OS ÏàËÆ¶È:55% Chinese Chemical Letters 2008 19 1427-1430 Synthesis and evaluation of in vitro antibacterial activity of novel 2,5-disubstituted-1£¬3£¬4-thiadiazoles from fatty acids Mudasir R£®Banday,Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ethyl linoleate C33H42O19 ÏàËÆ¶È:55% Natural Product Research 1995 7 35-41 New Cytotoxic Fatty Acid from Desmos cochinchinensis (Annonaceae) Nan-Jun Sun; David K. Ho; X. Eric Hu; Jeffrey M. Sneddon; Ralph E. Stephens; John M. Cassady Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . linderanolide A C19H30O3 ÏàËÆ¶È:55% Phytochemistry 1995 40 1175-1181 Linderanolides and isolinderanolides, ten butanolides from Lindera glauca Katsura Seki, Takayuki Sasaki, Satoshi Wano, Kazuo Haga, Ryohei Kaneko Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . isolinderanolide A C19H30O3 ÏàËÆ¶È:55% Phytochemistry 1995 40 1175-1181 Linderanolides and isolinderanolides, ten butanolides from Lindera glauca Katsura Seki, Takayuki Sasaki, Satoshi Wano, Kazuo Haga, Ryohei Kaneko Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1-[1'-(Decylsulfanyl)-3-phenylprop-2-ynyl]benzene C25H32S ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2011 59(9) 1133-1140 Lewis Acid-Catalyzed Propargylic Etherification and Sulfanylation from Alcohols in MeNO2¨CH2O Katsuki OHTA, Eri KOKETSU, Yuya NAGASE, Nami TAKAHASHI, Hiroyasu WATANABE, and Mitsuhiro YOSHIMATSU Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3,4'-bis(6-bromohexyl)-2,2'-bithiophene C20H28Br2S2 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2009 57 710-713 Clean and Direct Synthesis of ¦Á,¦Á¡ä-Bithiophenes and Bipyrroles by Metal-Free Oxidative Coupling Using Recyclable Hypervalent Iodine(III) Reagents Toshifumi Dohi, Koji Morimoto, Chieko Ogawa, Hiromichi Fujioka and Yasuyuki Kita Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 4-phenyl-1-(undec-10-enoyl)-thiosemicarbazide C18H27N3OS ÏàËÆ¶È:55% Indian Journal of Chemistry Section B 2009 48B 97-102 Substituted 1,2,4-triazoles and thiazolidinones from fatty acids: Spectral characterization and antimicrobial activity Banday,Mudasir Rashid; Rauf,Abdul Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (9Z)-4-phenyl-1-(octadec-9-enoyl)-thiosemicarbazide C25H41N3OS ÏàËÆ¶È:55% Indian Journal of Chemistry Section B 2009 48B 97-102 Substituted 1,2,4-triazoles and thiazolidinones from fatty acids: Spectral characterization and antimicrobial activity Banday,Mudasir Rashid; Rauf,Abdul Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . compound 4a C22H27N3 ÏàËÆ¶È:55% Heterocycles 2009 78 645-655 Copper(I)-Catalyzed Direct Arylation of 1,4-Disubstituted 1,2,3-Triazoles with Aryl Iodides Shin-ichi Fukuzawa, Eiji Shimizu, and Kenichi Ogata Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 6c C23H29N3 ÏàËÆ¶È:55% Heterocycles 2009 78 645-655 Copper(I)-Catalyzed Direct Arylation of 1,4-Disubstituted 1,2,3-Triazoles with Aryl Iodides Shin-ichi Fukuzawa, Eiji Shimizu, and Kenichi Ogata Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 4h C21H19ClN4O2S ÏàËÆ¶È:55% Heterocycles 2008 75 87-93 An Efficient Three-Component, One-Pot Synthesis of New Pyrimido[4, 5-d]pyrimidine-2, 4-diones Minoo Dabiri, Seyyedeh Cobra Azimi, Hamid Arvin-Nezhad, and Ayoob Bazgir Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 1-(Undec-10-enoyl)-5-phenylsemicarbazides ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry Letters 2010 20 1933-1938 Synthesis, characterization, and in vitro antimicrobial activities of 5-alkenyl/hydroxyalkenyl-2-phenylamine-1,3,4-oxadiazoles and thiadiazoles Nida N. Farshori, Mudasir R. Banday, Anis Ahmad, Asad U. Khan, Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 5-(8'Z)(heptadec-8'-enyl)-2-Phenylamine-1,3,4-thiadiazole ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry Letters 2010 20 1933-1938 Synthesis, characterization, and in vitro antimicrobial activities of 5-alkenyl/hydroxyalkenyl-2-phenylamine-1,3,4-oxadiazoles and thiadiazoles Nida N. Farshori, Mudasir R. Banday, Anis Ahmad, Asad U. Khan, Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 11-(Phenyl)-undec-10-ynoic acid benzylamide ÏàËÆ¶È:55% Archiv der Pharmazie 2007 340 154-158 Synthesis and Biological Evaluation of New Niphathesine Analogues J¨¹rgen Krauss, Christine Wetzel, Julia Thiel, Christine Neudert and Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . Methyi-(Z,E)-10,12-tetradecadienoate ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 1997 5 1267-1274 Identification and biosynthesis of (E,E)-10,12-tetradecadienyl acetate in Spodoptera littoralis female sex pheromone gland Isabel Navarro, Esther Mas, Gemma Fabri¨¤s, Francisco Camps Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . (13Z)-Icos-13-en-2-yn-1-ol ÏàËÆ¶È:55% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . (2E,13Z)-Icosa-2,13-dien-1-ol ÏàËÆ¶È:55% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . (2E,13E)-Icosa-2,13-dien-1-ol ÏàËÆ¶È:55% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . (2E,13Z)-Icosa-2,13-dienal ÏàËÆ¶È:55% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . (3RS,4E,15E)-Docosa-4,15-dien-1-yn-3-ol C22H38O ÏàËÆ¶È:55% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . ¦Á-linolenic acid C18H30O2 ÏàËÆ¶È:55% Bioscience, Biotechnology, and Biochemistry 2005 69 2186-2192 Isolation and Structure Determination of Algicidal Compounds from Ulva fasciata Mochammad Amin ALAMSJAH, Shotaro HIRAO, Fumito ISHIBASHI and Yuji FUJITA Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (Z,Z)-7,15-tetracosadiene-1,24-diol C24H46O2 ÏàËÆ¶È:55% Tetrahedron 2000 56 7633-7641 Bruchins¡ªMitogenic 3-(Hydroxypropanoyl) Esters of Long Chain Diols from Weevils of the Bruchidae James E Oliver, Robert P Doss, R.Thomas Williamson, John R Carney, E.David DeVilbiss Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . (8E,12Z)-9-allylicosa-8,12-diene C23H42 ÏàËÆ¶È:55% Russian Journal of Organic Chemistry 2007 43 956-960 Stereoselective synthesis of trisubstituted olefins through 2,5-dialkylidenemagnesacyclopentanes V. A. D¡¯yakonov, R. A. Zinnurova, A. G. Ibragimov and U. M. Dzhemilev Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 3,4'-bis(6-bromohexyl)-2,2'-bithiophene C20H28Br2S2 ÏàËÆ¶È:55% European Journal of Organic Chemistry 2011 6326-6334 etal-Free Oxidative Coupling Reactions via ¦Ò-Iodonium Intermediates: The Efficient Synthesis of Bithiophenes Using Hypervalent Iodine Reagents Koji Morimoto, Tomofumi Nakae, Nobutaka Yamaoka, Toshifumi Dohi and Yasuyuki Kita Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 5,6-dihydro-1-[2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethyl]-[1,2,3]triazolo[5,1-a]isoquinoline C20H18N6 ÏàËÆ¶È:55% Tetrahedron 2012 68 10310-10317 An easy access to 4-(1,2,3-triazolylalkyl)-1,2,3-triazole-fused dihydroisoquinolines and dihydroisoindoles Vito Fiandanese, Isabella Marino, Angela Punzi Structure 13C NMR ̼Æ×Ä£Äâͼ |

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