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1 . compound 4 C10H16O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1994 42 736-738 ABSOLUTE STEREOSTRUCTURES OF PAEONISOTHUJONE, A NOVEL SKELETAL MONOTERPENE KETONE, AND DEOXYPAEONISUFFRONE, AND ISOPAEONISUFFRAL, TWO NEW MONOTERPENES, FROM MOUTAN CORTEX Masayuki YOSHIKAWA,Emiko HARADA,Toshie MINEMATSU,Osamu MURAOKA,Johji YAMAHARA,Nobutoshi MURAKAMI and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3R,4S)-4-Hydroxymethyl-3-tert-butoxycarbonylamino-2,2-dimethyl-4-pentanolide ÏàËÆ¶È:60% Tetrahedron Letters 2003 44 9189-9192 Study of the Lewis acid-promoted addition of silylenol ethers to imines derived from glyceraldehyde Ram¨®n Badorrey, Carlos Cativiela, Marı́a D. Dı́az-de-Villegas, Jos¨¦ A. G¨¢lvez Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . N-tert-Butoxycarbonylleucine 2,2,2-trichloroethyl ester C13H22Cl3NO4 ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 1996 1427-1433 Synthesis of derivatives of (2S,4S)-4-hydroxy-2,5-dimethyl-3-oxohexanoic acid, a constituent of the didemnins Isabel Gonz¨¢lez, Gemma Jou, Josep Maria Caba, Fernando Albericio, Paul Lloyd-Williams and Ernest Giralt Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-piperidino-1-but-2-yn-1-yl propionate C12H19NO2 ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2011 47 161-167 Aminomethylation of acetylene alcohols and their esters with gem-diamines catalyzed by complexes of d-transition and rare-earth metals M. G. Shaibakova, I. G. Titova, A. G. Ibragimov and U. M. Dzhemilev Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . tert-Butyl N-(4-aminobutyl)-N-(3-hydroxypropyl)dicar-bamate C17H34N2O5 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2000 8 2059-2065 Synthesis and antimicrobial activity of squalamine analogue Hong-Seok Kim, Bo-Seung Choi, Kyung-Chan Kwon, Sang-Ok Lee, Hyun Jung Kwak, Cheol Hae Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N1,N3-Bis(tert-butoxycarbonyl)-N1-(5-bromopentyl)propane-1,3-diamine C18H35N2O4Br ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2013 21 4530-4540 Synthesis and evaluation of N8-acetylspermidine analogues as inhibitors of bacterial acetylpolyamine amidohydrolase Christophe Decroos, Christine M. Bowman, David W. Christianson Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3S,6S)-tert-butyl 2-(iodomethyl)-6-isobutyl-3-isopropyl-5-oxopiperazine-1-carboxylate C17H31IN2O3 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 10114-10121 An efficient entry to highly substituted chiral 2-oxopiperazines from ¦Á-amino acids via iodocyclization Amit Kumar Jana, Sanjit Kumar Das, Gautam Panda Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3R,6R)-tert-butyl 2-(iodomethyl)-6-isobutyl-3-isopropyl-5-oxopiperazine-1-carboxylate C17H31IN2O3 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 10114-10121 An efficient entry to highly substituted chiral 2-oxopiperazines from ¦Á-amino acids via iodocyclization Amit Kumar Jana, Sanjit Kumar Das, Gautam Panda Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 3 C10H16O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1994 42 736-738 ABSOLUTE STEREOSTRUCTURES OF PAEONISOTHUJONE, A NOVEL SKELETAL MONOTERPENE KETONE, AND DEOXYPAEONISUFFRONE, AND ISOPAEONISUFFRAL, TWO NEW MONOTERPENES, FROM MOUTAN CORTEX Masayuki YOSHIKAWA,Emiko HARADA,Toshie MINEMATSU,Osamu MURAOKA,Johji YAMAHARA,Nobutoshi MURAKAMI and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gelsemide ÏàËÆ¶È:50% Natural Product Research 1994 5 15-20 Two New Iridoids from the Leaves of Gelsemium elegans Benth. in Thailand Hiromitsu Takayama; Yuhko Morohoshi; Mariko Kitajima; Norio Aimi; Sumphan Wongseripipatana; Dhavadee Ponglux; Shin-Ichiro Sakai Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (2S)-4-azido-1,2-isopropylidendioxy-2-methylbutan C8H15N3O2 ÏàËÆ¶È:50% Helvetica Chimica Acta 1977 60 1273-1295 Stereoselektivitt und Reaktivitt bei der 1,3-dipolaren Cycloaddition chiraler N-(Alkoxyalkyl)nitrone Andrea Vasella Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N-acetyl-di[(3S)-3,4-isopropylidendioxy-3-methyl-1-butyl]amin ÏàËÆ¶È:50% Helvetica Chimica Acta 1977 60 1273-1295 Stereoselektivitt und Reaktivitt bei der 1,3-dipolaren Cycloaddition chiraler N-(Alkoxyalkyl)nitrone Andrea Vasella Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N-(1-Oxaspiro[5.5]undec-4-yl)acetamide C12H21NO2 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2009 87 698-705 Cerium(IV) sulfate catalyzed one-pot threecomponent diastereo selective synthesis of 4-amidotetrahydropyrans Nagarajan Panneer Selvam and Paramasivan T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 7b ÏàËÆ¶È:50% Organic letters 2001 3 1701-1704 Highly Enantioselective Hydrogenation of (E)-¦Â-(Acylamino)acrylates Catalyzed by Rh(I)-Complexes of Electron-Rich P-Chirogenic Diphosphines Masaya Yasutake, Ilya D. Gridnev, Natsuka Higashi, and Tsuneo Imamoto Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4,5-Dihydroxy-2,2,4-trimethylcyclopentanone ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 111-117 Alternative Synthesis of 2-Hydroxy-3,5,5-trimethylcyclopent-2-en-1-one Christian Chapuis and Christine Saint-L¨¦ger Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Compound 11 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2010 48 651-655 NMR studies on chiral intermediates in the total synthesis of (+)-biotin from D-mannose (pages 651¨C655) Wen-xue Chen, Ping Zhang and Fen-er Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Compound 12 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2010 48 651-655 NMR studies on chiral intermediates in the total synthesis of (+)-biotin from D-mannose (pages 651¨C655) Wen-xue Chen, Ping Zhang and Fen-er Chen Structure 13C NMR ̼Æ×Ä£Äâͼ |
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1 . citocalasina B ÏàËÆ¶È:77.7% Qu¨ªmica Nova 2005 28 991-995 Antifungal compounds of Xylaria sp., an endophytic fungus isolated from Palicourea marcgravii (Rubiaceae) Caf¨ºu, Mariana C.; Silva, Geraldo H.; Teles, Helder L.; Bolzani, Vanderlan da S.; Ara¨²jo, Ângela R.; Young, Maria Cl¨¢udia M.; Pfenning, Ludwig H. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cytochalasin F ÏàËÆ¶È:75.8% Journal of Natural Products 1999 62 155-157 Geniculol, a New Biologically Active Diterpene from the Endophytic Fungus Geniculosporium sp. Gabriele M. König, Anthony D. Wright, Hans-J. Aust, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 20-Deoxycytochalasin F C29H37NO4 ÏàËÆ¶È:70.3% Bioorganic & Medicinal Chemistry Letters 2012 22 3126-3129 Cytotoxic cytochalasins from the endozoic fungus Phoma sp. of the giant jellyfish Nemopilema nomurai Eun La Kim, Jian Lin Li, Hung The Dang, Jongki Hong, Chong-Ok Lee, Dong-Kyoo Kim,Won Duk Yoon, Euikyung Kim, Yonghong Liu, Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cytochalasin Z6 C29H37NO5 ÏàËÆ¶È:65.5% Journal of Natural Products 2003 66 1540-1544 Cytochalasins Z4, Z5, and Z6, Three New 24-Oxa[14]cytochalasans Produced by Phoma exigua var. heteromorpha Antonio Evidente,Anna Andolfi, Maurizio Vurro, Maria Chiara Zonno,and Andrea Motta Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-(n-butyl)amino-3-(4-fluorophenyl)-6,8-diphenyl-7-methyl-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]-pyrimidin-4(3H)-one C32H31FN4OS ÏàËÆ¶È:60.7% Journal of Heterocyclic Chemistry 2008 45 1809-1813 An efficient synthesis of new pyrido[4',3':4,5]thieno[2,3-d]-pyrimidin-4(3H)-one derivatives Yang-Gen Hu,Ming-Wu Ding and Guo-Ping Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cytochalasin W C29H33NO5 ÏàËÆ¶È:60% Natural Toxins 1996 4 53-57 Cytochalasin W, a new 24-oxa[14]cytochalasan from phoma exigua var. heteromorpha (pages 53¨C57) Antonio Evidente, Renato Capasso, Maurizio Vurro and Antonio Bottalico Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 20 C31H33O5 ÏàËÆ¶È:59.2% Phytochemistry 2001 58 775-787 Synthesis and antifeedant properties of N-benzoylphenylisoserinates of Lactarius sesquiterpenoid alcohols Piotr Kopczacki, Maria Gumu ka, Marek Masnyk, Halina Grabarczyk,Gerard Nowak, W odzimierz M. Daniewski Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . bitungolide F C24H32O4 ÏàËÆ¶È:59.2% Journal of Natural Products 2002 65 1820-1823 Bitungolides A-F, New Polyketides from the Indonesian Sponge Theonella cf. swinhoei Sodngam Sirirath,Junichi Tanaka, Ikuko I. Ohtani, Toshio Ichiba, Rachmaniar Rachmat, Kazunori Ueda,Takeo Usui, Hiroyuki Osada, and Tatsuo Higa Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . cytochalasin B ÏàËÆ¶È:59.2% China Journal of Chinese Materia Medica 2009 34 2060-2062 Chemical constituents in the introduced Coleus forskohlii ZHANG Weiwei, KONG Lingyi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-(4-methoxyphenyl)-3,3-bis(4-methylphenyl)-1'-methyl-spiro-[azetidine-2,3'-indoline]-2',4-dione C32H28N2O3 ÏàËÆ¶È:59.2% Journal of Heterocyclic Chemistry 2006 43 1665-1668 Reactions of ¦Á-diazoketones with indolinone imines: Synthesis of new 1,3,3-triaryl-1'-methylspiro[azetidine-2,3'-indoline]-2',4-diones Girija S. Singh and Boycie J. Mmolotsi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 16R,20R)-21,22-epoxy-7,20-dihydroxy-10-phenyl-24-oxa-[14]cytochalasa-6,13E,21E-diene-1,23-dione C29H37NO6 ÏàËÆ¶È:59.2% Magnetic Resonance in Chemistry 2008 46 650-659 Synthesis, complete 1H and 13C NMR assignment and crystal structure of novel epoxide derivatives of cytochalasin B (pages 650¨C659) Pieter S. Steyn, Jaco C. Breytenbach, Jeanne H. Botha, Manuel A. Fernandes and Philippus L. Wessels Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . splenocin B C28H32N2O9 ÏàËÆ¶È:59.2% Journal of Medicinal Chemistry 2009 52 2317-2327 Potent Inhibitors of Pro-Inflammatory Cytokine Production Produced by a Marine-Derived Bacterium Wendy K. Strangman, Hak Cheol Kwon, David Broide, Paul R. Jensen and William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (R)-3,3,3-trifluoro-2-methoxy-1-((S)-3-methylpiperidin-1-yl)-2-phenylpropan-1-one ÏàËÆ¶È:59.2% Tetrahedron 2012 68 10218-10229 A [3+3] cyclization strategy for asymmetric synthesis of alkyl substituted piperidine-2-ones using 1,2-cyclic sulfamidates: a formal synthesis of (S)-coniine from l-norvaline Abdullah Karanfil, Berrin Balta, Mustafa Eskici Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cytochalasin Z5 C29H37NO6 ÏàËÆ¶È:58.6% Journal of Natural Products 2003 66 1540-1544 Cytochalasins Z4, Z5, and Z6, Three New 24-Oxa[14]cytochalasans Produced by Phoma exigua var. heteromorpha Antonio Evidente,Anna Andolfi, Maurizio Vurro, Maria Chiara Zonno,and Andrea Motta Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Cytochalasin M ÏàËÆ¶È:57.1% Tetrahedron letters 1981 22 2703-2706 Structures of cytochalasin k, l and m, isolated from chalara microspora Tomas Fex Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . stoloniolide I C28H42O3 ÏàËÆ¶È:57.1% Chemistry Letters 1995 24 331-331 Structure of Sargassumketone, a Novel Highly Oxygenated Ketone from Sargassum Kjellmanianum Hiroshi Nozaki, Susumu Ohira, Daisuke Takaoka, Naoto Senda and Mitsuru Nakayama Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . L-696,475 C30H39NO3 ÏàËÆ¶È:57.1% The Journal of Antibiotics 1992 45 679-685 L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE II. ISOLATION AND STRUCTURE J. ONDEYKA, O. D. HENSENS, D. ZINK, R. BALL, R. B. LINGHAM, G. BILLS, A. DOMBROWSKI, M. GOETZ Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Cytochalasin H2 C32H43NO5 ÏàËÆ¶È:56.2% Records of Natural Products 2012 6 121-126 Cytochalasin H2,a New Cytochalasin,Isolated from the Endophytic Fungus Xylaria sp. A23 Yu Li,Chunhua Lu,Yaojian Huang,Yaoyao Li and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ |
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