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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
3Â¥2013-08-19 21:12:44
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-19 21:12:28
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