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341176

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̼Æ×Êý¾Ý£ºÈܼÁ,ë®´ú¼×´¼£º167.82, 158.70, 156.26, 137.30, 131.18, 104.36, 102.04, 81.25, 78.73, 74.48, 60.73, 56.25, 39.01, 38.04, 19.13, 13.97
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341176: ½ð±Ò+2, ¡ïÓаïÖú, ¸Ð¾õ²»ÊǺÜÏêϸ£¬²»¹ý»¹ÊÇллÁË£¬ÐÁ¿àÁË 2014-07-02 10:28:21
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1 .     drimane-3,8,11,12-tetraol
C15H28O4     ÏàËÆ¶È:50%
Mycology          2011          2          30-36
New sesquiterpenes from Marasmius cladophyllus
Jin Meng, Yao-Yao Li, Yi-Xin Ou, Long-Feng Song, Chun-Hua Lu & Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥2014-07-02 10:08:46
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341176

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2Â¥: Originally posted by ·çÐÐÕß007 at 2014-07-02 10:08:46
²éѯ½á¹û£º¹²²éµ½1¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     drimane-3,8,11,12-tetraol
C15H28O4     ÏàËÆ¶È:50%
Mycology          2011          2          30-36
New sesquiterpenes from Marasmius cladoph ...

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3Â¥2014-07-02 10:16:18
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3Â¥: Originally posted by 341176 at 2014-07-02 10:16:18
ÄãºÃ£¬Äܲ»ÄÜÔÙ¸øµÄÏêϸһµã£¬Ð»Ð»°¡ ºÙºÙ...

ÈܼÁÊÇë®´ú¼×´¼²éµ½µÄÖ»ÓÐÒ»ÖÖ£¬ÎÒÏÖÔÚ¸øÄãÓÃÈ«²¿ÈܼÁ²éµÄ½á¹û
²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     monocerin
    ÏàËÆ¶È:100%
Journal of Natural Products          2008          71(6)          1078-1081
Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi
Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     monocerin
C16H20O6     ÏàËÆ¶È:100%
Journal of Natural Products          2008          71(9)          1657-1659
11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum
Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (12S)-12-hydroxymonocerin
C16H20O7     ÏàËÆ¶È:81.2%
Journal of Natural Products          2008          71(6)          1078-1081
Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi
Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (12S)-12-hydroxymonocerin
C16H20O7     ÏàËÆ¶È:81.2%
Tetrahedron          2013          69          11025-11030
Biomimetically inspired total synthesis of (12S)-12-hydroxymonocerin and (12R)-12-hydroxymonocerin
Bowen Fang, Xingang Xie, Peng Jing, Changgui Zhao, Huilin Li, Haichen Ma, Xuegong She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (12S)-12-hydroxymonocerin
    ÏàËÆ¶È:81.2%
RSC Advances          2013          3          17717-17725
Total synthesis of (12R)- and (12S)-12-hydroxymonocerins: stereoselective oxylactonization using a chiral hypervalent iodine(III) species
Morifumi Fujita, Kazuhiro Mori, Mio Shimogaki and Takashi Sugimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (12R)-12-hydroxymonocerin
C16H20O7     ÏàËÆ¶È:75%
Journal of Natural Products          2008          71(6)          1078-1081
Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi
Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (12R)-12-hydroxymonocerin
C16H20O7     ÏàËÆ¶È:75%
Tetrahedron          2013          69          11025-11030
Biomimetically inspired total synthesis of (12S)-12-hydroxymonocerin and (12R)-12-hydroxymonocerin
Bowen Fang, Xingang Xie, Peng Jing, Changgui Zhao, Huilin Li, Haichen Ma, Xuegong She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (12R)-12-hydroxymonocerin
    ÏàËÆ¶È:75%
RSC Advances          2013          3          17717-17725
Total synthesis of (12R)- and (12S)-12-hydroxymonocerins: stereoselective oxylactonization using a chiral hypervalent iodine(III) species
Morifumi Fujita, Kazuhiro Mori, Mio Shimogaki and Takashi Sugimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     isocoumarin
C16H22O7     ÏàËÆ¶È:68.7%
Journal of Natural Products          2008          71(6)          1078-1081
Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi
Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     11-hydroxymonocerin
C16H20H7     ÏàËÆ¶È:68.7%
Journal of Natural Products          2008          71(9)          1657-1659
11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum
Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     diethyl 1-(4-methoxyphenyl)-2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
C26H28N2O7     ÏàËÆ¶È:56.2%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     diethyl 4-(4-chlorophenyl)-1-(4-methoxy-phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
C26H28ClNO5     ÏàËÆ¶È:56.2%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     diethyl 4-(furan-2-yl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
C24H27NO6     ÏàËÆ¶È:56.2%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 4
C18H22O7     ÏàËÆ¶È:55.5%
Journal of Natural Products          2008          71(9)          1657-1659
11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum
Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     diethyl 4-(2-cyanophenyl)-1-(4-methoxy-phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
C27H28N2O5     ÏàËÆ¶È:52.9%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     8¦Á,9¦Á-epoxyparthenolide
C15H18O4     ÏàËÆ¶È:50%
Fitoterapia          2004          75          573-576
Germacranolides from Anvillea radiata
B. El Hassany, F. El Hanbali, M. Akssira, F. Mellouki,A. Haidourb, A.F. Barrero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     6-methyl-7-acetyl-1,8-dihydroxy-3-methoxy naphthalene-1-O-¦Â-D(L)-glucoside
C20H25O9     ÏàËÆ¶È:50%
Molecules          2012          17          843-850
Two Novel Naphthalene Glucosides and an Anthraquinone Isolated from Rumex dentatus and Their Antiproliferation Activities in Four Cell Lines
Hui Zhang, Zengjun Guo, Nan Wu, Wenming Xu, Ling Han, Nan Li and Yanxia Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     diethyl 1,4-dihydro-2,6-dimethyl-4-(4-methoxyphenyl)pyridine-3,5-dicarboxylate
C20H25NO5     ÏàËÆ¶È:50%
Indian Journal of Chemistry Section B          2007          46B          331-335
Cu(OTf)₂ Catalyzed high yield synthesis of Hantzsch 1,4-dihydropyridines
Paraskar,Abhimanyu S; Sudalai,Arumugam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     diethyl 1,4-dihydro-2,6-dimethyl-4-(2-methoxyphenyl)pyridine-3,5-dicarboxylate
C20H25NO5     ÏàËÆ¶È:50%
Indian Journal of Chemistry Section B          2007          46B          331-335
Cu(OTf)₂ Catalyzed high yield synthesis of Hantzsch 1,4-dihydropyridines
Paraskar,Abhimanyu S; Sudalai,Arumugam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ethyl 6-methoxy-3-methylquinaldate
C14H15NO3     ÏàËÆ¶È:50%
Heterocycles          2005          66          611-619
One-Step Synthesis of Ethyl Quinaldates by Lewis Acid Catalyzed Three-Component Coupling Reaction of Aromatic Amines, Aliphatic Aldehydes and Ethyl Glyoxylate
Takashi Inada, Takayuki Nakajima, and Isao Shimizu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     torachrysone-8-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:50%
Journal of Shenyang Pharmaceutical University          2009          26          536-538
Chemical cnstituents of Caulis Polygoni Multiflori (the stem of Polygonum multif lorum Thunb.)
LIANG Yan, TIAN Wei-xi, MA Xiao-feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Phomopsinone A
C12H16O4     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2012                   1783-1789
Phomopsinones A¨CD: Four New Pyrenocines from Endophytic Fungus Phomopsis sp.
Hidayat Hussain, Karsten Krohn, Ishtiaq Ahmed, Siegfried Draeger, Barbara Schulz, Sebastiano Di Pietro and Gennaro Pescitelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     curvupallide A
C14H17NO5     ÏàËÆ¶È:50%
Tetrahedron          1995          51          4947-4952
Curvupallides, a new class of alkaloids from the fungus Curvularia pallescens
Wolf-Rainer Abraham, Holger Meyer, Dawit Abate
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     6-(4-bromobenzyl)-5-ethyl-2-(4-methoxyphenylcarbonylmethylthio)pyrimidin-4(3H)-one
C22H21BrN2O3S     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2008          16          3887-3894
Synthesis and biological evaluation of novel 6-substituted 5-alkyl-2-(arylcarbonylmethylthio)pyrimidin-4(3H)-ones as potent non-nucleoside HIV-1 reverse transcriptase inhibitors
Yue-Ping Wang, Fen-Er Chen, Erik De Clercq, Jan Balzarini, Christophe Pannecouque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (R)-ethyl 2-(3-methoxyphenoxy)propanoate
    ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2011                   176-182
Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis
Liwei Zhao, Zhong Li and Thomas Wirth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 8
C21H26O9S     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2010                   5100-5107
Formal Total Synthesis of (¨C)-Raphidecursinol B
Sanjit Kumar Das, Sajal Kumar Das and Gautam Panda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4-ethyl 3,5-dimethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate
C21H25NO7     ÏàËÆ¶È:50%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     triethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate
C23H29NO7     ÏàËÆ¶È:50%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     4-ethyl 3,5-diisopropyl 1-(4-methoxyphen-yl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate
C25H33NO7     ÏàËÆ¶È:50%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     3,5-dibenzyl 4-ethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate
C33H33NO7     ÏàËÆ¶È:50%
Tetrahedron          2013          69          5242-5247
Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite
Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     drimane-3,8,11,12-tetraol
C15H28O4     ÏàËÆ¶È:50%
Mycology          2011          2          30-36
New sesquiterpenes from Marasmius cladophyllus
Jin Meng, Yao-Yao Li, Yi-Xin Ou, Long-Feng Song, Chun-Hua Lu & Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ethyl 3-(4-cyano-3-hydroxy-5-{[(4-methylphenyl)methyl]sulfanyl}thiophen-2-yl)-3-oxopropanoate
C18H17NO4S2     ÏàËÆ¶È:50%
Tetrahedron          2013          69          9648-9655
New regio-selective method of combinatorial synthesis of substituted thiophenes, thieno[3,2-b]pyridines and other heterocycles via combination of ¡®domino¡¯-type reactions Original Research Article
Andrey A. Zubarev, Anatoliy M. Shestopalov, Natalia A. Larionova, Lyudmila A. Rodinovskaya, Alexander A. Shestopalov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     N,N-diethyl-4-(tert-butyldimethylsilyloxy)-6-iodo-1,3-benzodioxole-5-carboxamide
C18H28INO4Si     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2009          2009          4666-4673
Convergent Synthesis of Pancratistatin from Piperonal and Xylose
Johan Hygum Dam and Robert Madsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     2-¦Â-D-glucopyranosyloxy-6-methoxybenzoate
    ÏàËÆ¶È:50%
Shoyakugaku Zasshi          1991          45          255-260
Studies on the Chemical Constituents of Gloriosa rothschildiana and Colchicum autumnale
MIMAKI YOSHIHIRO, ISHIBASHI NAOKO, KOMATSU MUTSUMI, SASHIDA YUTAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     compound 7d
    ÏàËÆ¶È:50%
Chemical Journal of Chinese Universities          2013          34          2745-2751
Design, Synthesis and Activity Evaluation of N-Substituted Phthalimide Derivatives
QIN Si-Ning, Lv Wen-Wen, WANG Quan, ZHAO Qing-Chun*, XU Yong-Nan, *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4Â¥2014-07-02 10:36:41
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