| ²é¿´: 385 | »Ø¸´: 1 | ||
yy·¢½Í³ØÐ³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»À² ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï̼Æ×£º13.5, CH3£¬14.3, CH3£¬20.4, CH3£¬20.6, CH3£¬42.1, CH2£¬47.9, C£¬52.6, C£¬61.5, CH£¬62.3, CH£¬84.5, C£¬90.1, C£¬130.2, C£¬145.0, C£¬175.2, C£¬189.6, C ÈܼÁ£ºDMSO-d6 |
» 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:
ºË´Å̼Æ×ÇóÖú £¬ÈܼÁDMSO, 125M
ÒѾÓÐ4È˻ظ´
HETEROCYCLESͶ¸åÇóÖú
ÒѾÓÐ9È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
ºìÍâÏàËÆ¶ÈÇóÖú
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
΢Æ×Ò»¸ö£¬ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±ÇóÇóÖú΢Æ×Êý¾Ý¼ìË÷CÆ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
Ãâ·ÑµÄÆ×ͼÊý¾Ý¿â20¸ö
ÒѾÓÐ42È˻ظ´
÷´º
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 242 (´óѧÉú)
- ½ð±Ò: 1940.6
- É¢½ð: 48
- ºì»¨: 3
- Ìû×Ó: 465
- ÔÚÏß: 121.1Сʱ
- ³æºÅ: 1536801
- ×¢²á: 2011-12-14
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yy·¢½Í³Ø: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-17 14:38:29
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yy·¢½Í³Ø: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-17 14:38:29
|
1 . picrotoxic acid C15H18O7 ÏàËÆ¶È:60% Phytochemistry 1999 51 1365-1368 Two picrotoxin derivatives from Anamirta cocculus Santosh K.Agarwal, Sudhir S. Singh, Sushma Verma, Sushil Kumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 2g C16H29N2O6P ÏàËÆ¶È:60% Heterocycles 2012 85 2765-2774 Behaviour of ¦Â-Keto-¦Ä-carbethoxyphosphonates and Phosphine Oxides in the Biginelli Multicomponent Reaction: Regioselective Synthesis of 5-Carbethoxy-6-phosphonomethyl-3,4-dihydropyrimidin-2-ones Emna Chebil and Soufiane Touil Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Ethyl N-(2-chloro-5-nitrobenzyl)leucinate C15H21ClN2O4 ÏàËÆ¶È:60% Monatshefte f¨¹r Chemie 2014 145 483−489 Synthesis of N-carboxyalkyl-1,4-benzothiazepine-3(2H)-one derivatives using esters of N-(2-chloro-5-nitrobenzyl)amino acids Taras M. Tarasiuk, Tetiana A. Volovnenko, Yulian M. Volovenko, Volodymyr V. Medviediev, Oleg V. Shishkin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 1,10-epoxy-4-germacrene-12,8;15,6-diolide C15H20O5 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 925-928 Antiviral Constituents against Respiratory Viruses from Mikania micrantha Paul Pui-Hay But, Zhen-Dan He, Shuang-Cheng Ma, Yiu-Man Chan, Pang-Chui Shaw, Wen-Cai Ye,and Ren-Wang Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . salinosporamide H C15H21NO4 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 269-276 Salinosporamides D-J from the Marine Actinomycete Salinispora tropica, Bromosalinosporamide, and Thioester Derivatives Are Potent Inhibitors of the 20S Proteasome Katherine A. Reed, Rama Rao Manam, Scott S. Mitchell, Jianlin Xu, Sy Teisan, Ta-Hsiang Chao, Gordafaried Deyanat-Yazdi,Saskia T. C. Neuteboom, Kin S. Lam, and Barbara C. M. Potts Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . dihydrophaseic acid ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2009 45 545-546 COMPONENTS OF Sophora alopecuroides SEEDS Guan Ye, Chun-Hui Ma, Xiang-Yuan Huang,Zhi-Xiong Li, and Cheng-Gang Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2009 11 991-996 Stereoselective hydrogenation on the exocyclic and conjugated double bond of sesquiterpene lactones by Aspergillus versicolor D-1 Dan Wang, Li Yang, Hong Guan, Yi-Nan Chen, Wei-Zhuo Xu and Song You Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . sonchifolactone E C15H18O5 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2008 10 211-213 Two new compounds from Ixeris sonchifolia Nan Zhang, A-Li Lv, Zhe Zheng, Yi-Mei Zeng, Ying-Na Li and Yue-Hu Pei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 6-[(2-Oxopyrrolidin-1-yl)methyl]-9-(2-deoxy-¦Â-D-erythro-pentofuranosyl)purine C15H19N5O4 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2008 16 2329-2366 Synthesis, cytostatic and anti-HCV activity of 6-(N-substituted aminomethyl)-, 6-(O-substituted hydroxymethyl)- and 6-(S-substituted sulfanylmethyl)purine nucleosides Peter Šilh¨¢r, Michal Hocek, Radek Pohl, Ivan Votruba, I-hung Shih, Eric Mabery, Richard Mackman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Diethyl-1-methoxy-2-oxo-6,7-diazabicyclo[3.2.2]nona-3,8-diene-6,7-dicarboxylate ÏàËÆ¶È:53.3% Archiv der Pharmazie 2007 340 569-576 Synthesis and In Vitro Protozoocidal Evaluation of Novel Diazabicyclic Tropolone Derivatives Alexander Khrizman, Rachel D. Slack, Richard C. Remsing, Susan Little, Vanessa Yardley and Guillermo Moyna Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ethyl 4-acetyl-8-formyl-3,4-dihydro-6-methyl-2H-1,4-benzoxazine-2-carboxylate C15H17NO5 ÏàËÆ¶È:53.3% Heterocycles 2001 55 1873-1888 Regioselective Formylation of Ethyl 3,4-Dihydro-2H-1,4- benzoxazine-2-carboxylate or 2-Acetate Derivatives Stanislas Mayer, G¨¦rald Guillaumet, and Jean-Yves M¨¦rour Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 6-chloro-9-[(1R*,2R*,4R*)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]-9H-purine C15H19ClN4 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2010 18 4374-4384 Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors Michal Ѝ¢la, Armando M. De Palma, Hubert Hřebabecký, Radim Nencka, Martin Drač¨ªnský, Pieter Leyssen, Johan Neyts, Anton¨ªn Holý Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl (2E)-2-[2-(3,4-dimethylphenyl)-1-ethoxy-2-hydroxypropylidene]hydrazinecarboxylate C15H22N2O4 ÏàËÆ¶È:53.3% Archiv der Pharmazie 2011 344 755-764 Facile Synthesis and In-Vitro Antimalarial Activity of Novel -Hydroxy Hydrazonates (pages 755¨C764) Mehdi Khankischpur, Finn K. Hansen, Ronald Meurer, Tobias Mauz, Baerbel Bergmann, Rolf D. Walter and Detlef Geffken Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-hydroxy-1(10),3,11(13)-guaiatriene-12,6-olide-2-one ÏàËÆ¶È:53.3% Biotechnology Letters 2005 27 1189-1193 Newly Detected Specific Hydrogenation of the Conjugated Double Bond of Unsaturated Alkaloid Lactones by Aspergillus sp. Hong Guan, Song You, Li Yang, Xu Wang, Rui Ni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (Z)-ethyl (3-benzyl-5-methyl-4-oxothiazolidin-2-ylidene)ethanoate C15H17NO3S ÏàËÆ¶È:53.3% Tetrahedron 2013 69 6436-6447 2-Alkylidene-4-oxothiazolidine S-oxides: synthesis and stereochemistry Zdravko Džambaski, Rade Marković, Erich Kleinpeter, Marija Baranac-Stojanović Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ethyl (2S*,3R*)-3-benzamido-2-propylhexanoate C18H27NO3 ÏàËÆ¶È:53.3% Tetrahedron 2014 70 2515-2522 Stereocontrolled transformation of cyclohexene ¦Â-amino esters into syn- or anti-difunctionalized acyclic ¦Â2,3-amino acid derivatives Original Research Article Maria Cherepanova, Lor¨¢nd Kiss, Ferenc F¨¹löp Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-Deoxy-1-[2'-oxo-1'-pyrrolidinyl]-2-n-butyl-a-fructofuranoside C14H25NO6 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2012 14 528-532 Chemical constituents from the fruits of Trichosanthes kirilowii Xue-Mei Fan, Gang Chen, Yi Sha, Xuan Lu, Ming-Xi Shen, Hong-Mei Ma & Yue-Hu Pei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-[5-(ethoxycarbonyl)-6-methyl-2-oxo-4-phenyl-3,4-dihydropyrimidin-1(2H)-yl]pentanoic acid C19H24N2O5 ÏàËÆ¶È:52.9% Journal of Heterocyclic Chemistry 2013 50 1299-1303 Protecting Group Free Synthesis of Carboxyl-substituted Dihydropyrimidines Through Biginelli Reaction Eugeniy N. Ostapchuk, Andrey S. Plaskon, Oleksandr O. Grygorenko, Andrey A. Tolmachev and Sergey V. Ryabukhin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 5a C30H32N2O8 ÏàËÆ¶È:52.9% Tetrahedron 2014 70 2537-2545 Synthesis of complex dispirocyclopentanebisoxindoles via cycloaddition reactions of 4-dimethylamino-1-alkoxycarbonylmethylpyridinium bromides with 2-oxoindolin-3-ylidene derivatives Original Research Article Li-Juan Lu, Qin Fu, Jing Sun, Chao-Guo Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . Ethyl 3-methyl-1-(4-methylbenzyl)-4-oxo-1,4,5,7-tetrahydrothiopyrano[3,4-b]pyrrole-2-carboxylate C19H21NO3S ÏàËÆ¶È:52.9% Tetrahedron 2012 68 5087-5094 An efficient synthesis of pyrrolo[3¡ä,2¡ä:4,5]thiopyrano[3,2-b]pyridin-2-one: a new ring system of pharmaceutical interest Paola Barraja, Patrizia Diana, Virginia Span¨°, Alessandra Montalbano, Anna Carbone, Barbara Parrino, Girolamo Cirrincione Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-15 00:49:58














»Ø¸´´ËÂ¥