| ²é¿´: 206 | »Ø¸´: 1 | |||
zxb2007211ͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹ zq-H+ ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 21.62, 22.51, 22.54, 27.76, 29.02, 38.97, 42.86, 79.09, 119.33, 121.12, 126.36, 135.18, 156.11 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ17È˻ظ´
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ12È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ23È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÔÚÄĸöÍøÕ¾¿ÉÒԲ鵽»¯ºÏÎïµÄͼÆ×
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆ×Êý¾Ý£¬¿ÉÄÜÊǽṹºÜ¶Ô³ÆµÄ»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+2, ¹ÄÀøÓ¦Öú 2013-12-11 18:21:18
zxb2007211: ½ð±Ò+10 2013-12-12 11:59:09
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+2, ¹ÄÀøÓ¦Öú 2013-12-11 18:21:18
zxb2007211: ½ð±Ò+10 2013-12-12 11:59:09
|
²éѯ½á¹û£º¹²²éµ½137¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-sydonic acid C15H22O4 ÏàËÆ¶È:86.6% Chinese Journal of Marine Drugs 2012 31 7-13 Secondary metabolites and their bioactivities of a soft coral-derived fungus Aspergillus versicolor(ZJ-2008015) ZHENG Cai-juan; SHAO Chang-lun; WANG Kai-ling; ZHAO Dong-lin; WANG Ya-nan; WANG Chang-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6-(5-methylhex-2-enyl)-3,6-dihydropyran-2-one C12H18O2 ÏàËÆ¶È:76.9% European Journal of Organic Chemistry 2010 5063-5070 Regioselective Tandem Ring Closing/Cross Metathesis of 1,5-Hexadien-3-ol Derivatives: Application to the Total Synthesis of Rugulactone Fanny Cros, B¨¦atrice Pelotier and Olivier Piva Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-Isopropyl-2,4,4a,9-tetrahydro-3H-xanthene ÏàËÆ¶È:64.2% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 556-565 ALKYLATION OF PHENOL BY MYRTENOL A. A. Koroleva, I. Yu. Chukicheva,I. V. Fedorova, and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (S)-1-Cyano-N-[benzyloxycarbonyl]-N'-[tert-butyioxycarbonyl]-1,5-diaminopentane C19H27N3O4 ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry 1996 4 1185-1196 Salen-anthraquinone Conjugates. Synthesis, DNA-binding and cleaving properties, effects on topoisomerases and cytotoxicity Sylvain Routier, Nicole Cotelle, Jean-Pierre Catteau, Jean-Luc Bernier, Michael J. Waring, Jean-François Riou, Christian Bailly Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (S)-(+)-11-dehydrosydonic acid C15H20O4 ÏàËÆ¶È:60% Journal of Natural Products 2010 73 911-914 Cytotoxic Polyphenols from the Marine-Derived Fungus Penicillium expansum Zhenyu Lu, Huajie Zhu, Peng Fu, Yi Wang, Zhihua Zhang, Haipeng Lin, Peipei Liu, Yibin Zhuang, Kui Hong and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Phidianidine B C17H23N7O ÏàËÆ¶È:58.8% Organic Letters 2011 Vol.13,No.10 2516-2519 Structure and Cytotoxicity of Phidianidines A and B: First Finding of 1,2,4-Oxadiazole System in a Marine Natural Product Marianna Carbone,Yan Li, Carlo Irace, Ernesto Mollo, Francesco Castelluccio,Antonio Di Pascale, Guido Cimino,Rita Santamaria, Yue-Wei Guo, and Margherita Gavagnin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1S,6S)-Tetrazolo [1,5-g]-7-Aza-trans-himachal-2-ene ÏàËÆ¶È:57.1% Molecules 2001 6 M227 (1S, 6S)-Tetrazolo [1, 5-g]-7-Aza-trans-himachal-2-ene M. Dakir, E. Lassaba and A. Benharref Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 10b C16H22S ÏàËÆ¶È:57.1% Tetrahedron Letters 2002 43 9615-9619 Thermal rearrangements of bis-allenyl thiosulfonates. Synthesis of novel thienothiophene and thieno-oxathiine derivatives Mihail L. Birsa, Marina Cherkinsky, Samuel Braverman Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (S)-6-tert-butoxycarbonylamino-2-tosylamino-1-hexanol C18H30N2O5S ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2009 17 3463-3470 Synthesis and biological evaluation of reversible inhibitors of IdeS, a bacterial cysteine protease and virulence determinant Kristina Berggren, Björn Johansson, Tomas Fex, Jan Kihlberg, Lars Björck, Kristina Luthman Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (S)-1-azido-6-tert-butoxycarbonylamino-2-tosylamino-hexane C18H29N5O4S ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2009 17 3463-3470 Synthesis and biological evaluation of reversible inhibitors of IdeS, a bacterial cysteine protease and virulence determinant Kristina Berggren, Björn Johansson, Tomas Fex, Jan Kihlberg, Lars Björck, Kristina Luthman Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Amorpha-4,9-dien-2-ol ÏàËÆ¶È:53.8% Phytochemistry 2001 58 789-798 Sesquiterpenoid constituents of the liverworts Lepidozia fauriana and Lepidozia vitrea Claudia Paul, Wilfried A. König, Chia-Li Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . laughine C11H19N5OBr ÏàËÆ¶È:53.8% Journal of Natural Products 2005 68 327-330 Dominicin, a Cyclic Octapeptide, and Laughine, a Bromopyrrole Alkaloid, Isolated from the Caribbean Marine Sponge Eurypon laughlini David E. Williams, Brian O. Patrick, Hans W. Behrisch, Rob Van Soest, Michel Roberge, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-(2,3,4,9-tetrahydro-1H-¦Â-carbolin-1-yl)ethylamine ÏàËÆ¶È:53.8% Journal of Natural Products 1997 60 791-793 Reductive Pictet-Spengler Cyclization of Nitriles in the Presence of Tryptamine: Synthesis of Indolo[2, 3-a]quinolizidine, Nazlinine, and Elaeocarpidine Khalid Diker, Khalid El Biach, Mich¨¨le Dö¨¦de Maindreville, and Jean L¨¦vy Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Boc-leucyl(N`-benzoyl)-hydrazide C18H27N3O4 ÏàËÆ¶È:53.8% Molecules 2005 10 1218-1228 Synthesis and Biological Activity of Novel Amino Acid-(N'-Benzoyl) Hydrazide and Amino Acid-(N'-Nicotinoyl) Hydrazide Derivatives Sherine N. Khattab Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Boc-leucyl(N`-nicotinoyl)-hydrazide C17H26N4O4 ÏàËÆ¶È:53.8% Molecules 2005 10 1218-1228 Synthesis and Biological Activity of Novel Amino Acid-(N'-Benzoyl) Hydrazide and Amino Acid-(N'-Nicotinoyl) Hydrazide Derivatives Sherine N. Khattab Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 9,10-dihydroxynerylacetone ÏàËÆ¶È:53.8% Phytochemistry 1998 47 1025-1028 Biotransformation of (2Z,6Z)-farnesol by the plant pathogenic fungus Glomerella cingulata Hirokazu Nankai, Mitsuo Miyazawa, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (Z)-9,10-dihydroxy-6,10-dimethyl-5-undecen-2one C13H24O3 ÏàËÆ¶È:53.8% Phytochemistry 1995 40 1133-1137 Biotransformations of acyclic terpenoids, (¡À)-cis-nerolidol and nerylacetone, by plant pathogenic fungus, Glomerella cingulata Mitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2-[(cis-decal-9',2'-diyl)-hydroxy-methyl]imidazol C14H20N2O ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1978 61 2831-2842 Photochemische Reaktionen. 99. Mitteilung. Photochemistry of N-Acylimidazoles. IV. Structural Factors Leading to Norrish Type II Elimination and to Cyclobutanol Formation in the Photolysis of Acylimidazoles Shigeo Iwasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . tert-Butyl 2-(5-chloro-1H-indol-3-yl)-2-(hydroxyamino)-ethylcarbamate ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2011 19 3204-3215 Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents Olga N. Burchak,Emmanuelle Le Pihive, Laure Maigre, Xavier Guinchard , Pascale Bouhours ,Claude Jolivalt, Dominique Schneider , Max Maurin , Carmela Giglione , Thierry Meinnel ,Jean-Marc Paris , Jean-Noël Denis Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Cp*TiMe2[NP-t-Bu2(2-CH2Py)] ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 2006 84 755-761 Titanium pyridyl-phosphinimide complexes -Synthesis, structure, and ethylene polymerization catalysis Chad Beddie, Pingrong Wei, and Douglas W. Stephan Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . N-Pentylcarbazole ÏàËÆ¶È:53.8% Marine drugs 2011 9 256-277 Synthesis of 1-Substituted Carbazolyl-1,2,3,4-tetrahydro- and Carbazolyl-3,4-dihydro-¦Â-carboline Analogs as Potential Antitumor Agents Ya-Ching Shen,Yao-To Chang,Chun-Ling Lin,Chia-Ching Liaw,Yao Haur Kuo,Lan-Chun Tu,Sheau Farn Yeh and Ji-Wang Chern Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4-trifluoromethyl-5,6,7,8,9,10,11,12,13,14-decahydro-cyclododeca[d]-2(1H)pyrimidinone C15H23F3N2O ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2009 46 158-163 2-Trifluoroacetyl-1-methoxycycloalkenes: A convenient precursor for the synthesis of geminated polymethylene trifluoromethyl substituted heterocycles Helio Gauze Bonacorso,Michelle Budke Costa,Cleber Andr¨¦ Cechinel,Ronan Carlo Sehnem,Marcos Antonio Pinto Martins and Nilo Zanatta Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 7-[2'-(6-Oxoheptyl)-1H,1'H-5,5'-bibenzimidazolyl-2-yl]heptan- 2-one C28H34N4O2 ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2005 42 1001-1005 Reaction of 1,3-dicarbonyl compounds with o-phenylenediamine or 3,3'-diaminobenzidine in water or under solvent-free conditions via microwave irradiation Zhong-Xia Wang and Hua-Li Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 6-(p-tolyl)-cis-4,5-cyclohexa-1,4,5,6-tetrahydropyridazin-3(2H)-one C15H20N2O ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2004 41 259-261 Synthesis and structure of cycloalkane-and norbornane-condensed 6-aryl-1,2,4,5-tetrahydropyridazinones Ferenc Csende,Anaszt¨¢rzia Het¨¦nyi,G¨¦za St¨¢jer and Ferenc F¨¹löp Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-11 16:53:46














»Ø¸´´ËÂ¥