±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 305  |  »Ø¸´: 1

Ī֮¿¡

½ð³æ (ÕýʽдÊÖ)

[ÇóÖú] άÆ×Êý¾ÝÇóÖú ÒÑÓÐ1È˲ÎÓë

̼Æ×£º13C NMR (126 MHz, MeOD) ¦Ä 173.17, 157.12, 151.87, 150.06, 130.81, 128.62, 125.60, 115.79, 65.02, 40.65, 25.97, 14.02.
ллÀ²~~~~
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

×ö×Ô¼º¾ÍºÃ£¡
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

seuseasoar

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ī֮¿¡: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-18 15:39:52
1 .     1,4,5,6-Tetrahydro-3-methyl-1-(2-phenoxyacetyl)-cyclopenta[c]pyrazole
C15H16N2O2     ÏàËÆ¶È:61.5%
Tetrahedron          2003          59          4591-4601
Unusual reaction of N-aroyldihydrocyclopenta-pyrazolidinol with ketenes: formation of 1, 3, 4-oxadiazoles
Constantinos A Tsoleridis, Julia Stephanidou-Stephanatou, Petros Gounaridis, Hara Zika, Minodora Pozarentzi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     allyl 3-(2-hydroxyphenyl)propanoate
    ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2008          45          435-443
Synthesis of 1,3-oxazole and benzimidazole pendant groups from polyacrylonitrile hydrolysis products
Isabel N. Vega,Leonardo S¨¢nchez and Norma D'Accorso
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     methyl(¡À)-2-(2-nitrophenyl)-5-oxopentanoate
    ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2004          41          563-568
Diastereoselective synthesis of substituted 2,3,4,5-tetrahydro-1H-1-benzazepine-5-carboxylic esters by a tandem reduction-reductive animation reaction
Richard A. Bunce,Lara B. Johnson and Elizabeth M. Holt
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     compound 2e
    ÏàËÆ¶È:58.3%
Indian Journal of Chemistry Section B          2007          46B          204-206
Silica supported chromium trioxide: Microwave promoted oxidative ring closure of ¦Á-cyano-¦Â-thioenaminones to isothiazoles
Mishra,Manisha; Mahalanabis,Kumar K
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     6-Butyl-6-methyl-12H-dibenzo(d,g)(1,3)dioxocin
C19H22O2     ÏàËÆ¶È:58.3%
Tetrahedron Letters          2004          45          6909-6913
Indium(III) chloride catalyzed one step synthesis of some new dibenzo(d,f)(1,3)dioxepines and 12H-dibenzo(d,g)(1,3)dioxocin derivatives
Graziella Tocco, Michela Begala, Giovanna Delogu, Carmen Picciau, Gianni Podda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3-[2-(butan-2-ylidene)hydrazinyl]quinoxalin-2(1H)-one
C12H14N4O     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2010          18          214-221
Microwave assisted synthesis and antimicrobial activity of 2-quinoxalinone-3-hydrazone derivatives
Olayinka O. Ajani, Craig A. Obafemi, Obinna C. Nwinyi, David A. Akinpelu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     [2,6,2',6'-tetrahydroxy,4,4'-bis-(propionic acidhexyl ester)] biphenyl
    ÏàËÆ¶È:58.3%
Food Chemistry          2009          116          371-381
Isolation and structure elucidation of novel phenolic constituents from Sorbus domestica fruits
Aikaterini Termentzi, Maria Zervou, Eugene Kokkalou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     methyl 4-prenyloxyphenylacetate
C14H18O3     ÏàËÆ¶È:58.3%
Tetrahedron          2012          68          9592-9597
Unified route to asymmetrically substituted butenolide, maleic anhydride, and maleimide constituents of Antrodia camphorata
John Boukouvalas, Vincent Albert, Richard P. Loach, Raphaël Lafleur-Lambert
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     5-(6-bromo-2H-chromen-3-yl)-1H-tetrazole
C10H7N4OBr     ÏàËÆ¶È:58.3%
Tetrahedron          2013          69          1841-1848
The study of catalyst free and copper catalyzed reactions of cyanochromenes and sodium azide
Sachin D. Gawande, Mustafa J. Raihan, Manoj R. Zanwar, Veerababurao Kavala, Donala Janreddy, Chun-Wei Kuo, Mei-Ling Chen, Ting-Shen Kuo, Ching-Fa Yao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     4-fluoro-N-((2-phenyloxazol-5-yl)methyl)aniline
C16H13N2OF     ÏàËÆ¶È:58.3%
Chinese Chemical Letters          2013          24          957-961
Synthesis of novel 1,3-oxazole derivatives with insect growth-inhibiting activities
Peng Guo, Jun-Hai Huang, Qing-Chun Huang, Xu-Hong Qian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     methyl 3-(2-oxo-2H-benzo[1,4]oxazin-3-yl)propanoate
C12H11NO4     ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2013          50          413-416
Novel 3-(2-Oxo-2H-benzo[1,4]oxazin-3-yl)propanoates from Dimethyl-2-oxoglutarate and Test of Their Biological Activity
Kamel Hachama, Mohamed Khodja, Saad Moulay, Hocine Boutoumi, Lothar Hennig and Dieter Sicker
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     4-butoxy-benzeneacetic acid
    ÏàËÆ¶È:58.3%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2009          48(3)          136-138
Secondary Metabolites of Mangrove Endophytic Fungus B2 in the South China Sea
ZHANG Yi, YANG Chang, XU Fang, LIU Lan, LIN Yongcheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     1-¼×Ñõ»ù-2,3-±½²¢»·ÎìÍé
C10H12O     ÏàËÆ¶È:58.3%
Journal of Tropical and Subtropical Botany          2008          16          46-50
°×Í·Ê÷»¯Ñ§³É·ÖÑо¿
Òó˧ÎÄ, ºÎÐñ÷, Íõ±ó¹ó, ФÒ˰²
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     alnusdiol
    ÏàËÆ¶È:58.3%
Chinese Traditional and Herbal Drugs          2013          44          2650-2656
Chemical constituents in leaves of Ostryopsis nobilis and their anti-oxidant activities
FENG Meng-meng, ZHANG Yan-xia, XIA Bing, HE Da-hai, DING Li-sheng, ZHOU Yan, YE Xiao-xia
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Chloromethyl (coumarin-3-yl)carbamate
C11H8ClNO4     ÏàËÆ¶È:58.3%
European Journal of Medicinal Chemistry          2013          63          151-161
Novel (coumarin-3-yl)carbamates as selective MAO-B inhibitors: Synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study Original Research Article
Maria J. Matos, Santiago Vilar, Rosa Ma Gonzalez-Franco, Eugenio Uriarte, Lourdes Santana, Carol Friedman, Nicholas P. Tatonetti, Dolores Viña, Jose A. Fontenla
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
ÄáºÕ
2Â¥2015-03-17 23:21:09
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ Ī֮¿¡ µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] ¿¼Ñе÷¼Á +6 15615482637 2026-04-04 6/300 2026-04-04 22:43 by yu221
[¿¼ÑÐ] 320Çóµ÷¼Á +3 Ò»ÑùÔ² 2026-04-04 3/150 2026-04-04 22:29 by à£à£à£0119
[¿¼ÑÐ] Çóµ÷¼Á +7 xzghyuj 2026-04-04 7/350 2026-04-04 22:25 by oooqiao
[¿¼ÑÐ] 358Çóµ÷¼Á +5 Çïgk 2026-04-04 5/250 2026-04-04 21:03 by dongzh2009
[¿¼ÑÐ] 324Çóµ÷¼Á +14 ÏëÉÏѧÇóµ÷ 2026-04-02 15/750 2026-04-04 20:31 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] Ò»Ö¾Ô¸ÉϺ£´óѧÉúÎïѧ346 +3 ÉϺ£´óѧ346µ÷¼Á 2026-04-03 3/150 2026-04-04 20:20 by dongzh2009
[¿¼ÑÐ] 385·Ö ÉúÎïѧ£¨071000£©Çóµ÷¼Á +9 qf626 2026-04-01 9/450 2026-04-04 18:10 by macy2011
[¿¼ÑÐ] 085600£¬×¨Òµ¿Î»¯¹¤Ô­Àí£¬320·ÖÇóµ÷¼Á +8 ´ó²öС×Ó 2026-03-29 8/400 2026-04-04 16:21 by dongzh2009
[¿¼ÑÐ] Ò»Ö¾Ô¸±±½»´ó²ÄÁϹ¤³Ì×Ü·Ö358 +6 cs0106 2026-04-03 6/300 2026-04-04 11:20 by w_xuqing
[¿¼ÑÐ] Ò»Ö¾Ô¸Äϲý´óѧ324Çóµ÷¼Á +9 hanamiko 2026-03-30 9/450 2026-04-04 11:04 by Öí»á·É
[¿¼ÑÐ] 085600²ÄÁÏÓ뻯¹¤µ÷¼Á +26 kikiki7 2026-03-30 27/1350 2026-04-04 09:18 by qlm5820
[¿¼ÑÐ] Çóµ÷¼Á +4 ѹÁ¦??´ó 2026-04-03 4/200 2026-04-03 21:36 by à£à£à£0119
[¿¼ÑÐ] 085801 ×Ü·Ö275 ±¾¿ÆÐÂÄÜÔ´ Çóµ÷¼Á +19 bradoner 2026-04-01 23/1150 2026-04-03 10:07 by linyelide
[¿¼ÑÐ] 366Çóµ÷¼ÁÒ»Ö¾Ô¸¶«±±´óѧ +8 ÔËÆøÀ´µÃÈôÓÐËÆÎ 2026-04-02 8/400 2026-04-02 21:39 by dongzh2009
[¿¼ÑÐ] 377Çóµ÷¼Á +3 RASKIN 2026-04-02 3/150 2026-04-02 09:45 by zzchen2000
[¿¼ÑÐ] Ò»Ö¾Ô¸±±½»´ó²ÄÁϹ¤³Ì£¬×Ü·Ö358 +4 cs0106 2026-04-01 4/200 2026-04-02 07:42 by ÉÐË®¸óÖ÷
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +12 Ò»ÑùYWY 2026-04-01 12/600 2026-04-02 00:21 by °ÙÃë¹âÄê
[¿¼ÑÐ] 298Çóµ÷¼Á +4 ʲôÊÇÅÖÍ·Óã 2026-03-30 6/300 2026-04-01 22:06 by ¿Í¶ûÃÀµÂ
[¿¼ÑÐ] 318Çóµ÷¼Á +10 ³Â³¿79 2026-03-30 10/500 2026-03-31 17:37 by 544594351
[¿¼ÑÐ] 370Çóµ÷¼Á +3 080700µ÷¼Á 2026-03-30 3/150 2026-03-31 01:09 by A_Zhe
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û