±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 274  |  »Ø¸´: 1

Artclass

ľ³æ (СÓÐÃûÆø)

[ÇóÖú] ÇóÖú΢Æ×Êý¾Ý¡£Ð»Ð»

ÈܼÁΪ뮴úÂȷ£¬Ì¼Æ×Êý¾ÝÈçÏ£º

13.4, 50.5, 60.4, 77.0 83.0, 115.4, 124.5, 126.0, 126.8, 127.3, 127.7, 130.7, 134.8, 138.8, 147.3, 161.0, 171.5

×ܹ²17¸öC£¬Ð»Ð»~
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

ÓÐËù²»Îª

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Artclass: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-05 15:14:30
²éѯ½á¹û£º¹²²éµ½757¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     Chaetominine
C22H18N4O4     ÏàËÆ¶È:72.7%
Organic Letters          2006          8          5709-5712
Chaetominine, a Cytotoxic Alkaloid Produced by Endophytic Chaetomium sp. IFB-E015
Rui H. Jiao, Shu Xu,Jun Y. Liu, Hui M. Ge, Hui Ding, Chen Xu, Hai L. Zhu, and Ren X. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


2 .     (-)-chaetominine
     ÏàËÆ¶È:71.4%
Chinese Pharmaceutical Journal          2011          46          1154-1158
Metabolites of Aspergillus sp. HT-2
ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


3 .     ethyl 1-hydroxy-3-phenyl-2-naphthoate
C19H16O3     ÏàËÆ¶È:70.5%
Tetrahedron          2012          68          9035-9044
Silver-catalyzed regioselective synthesis of acridines, quinolines, and naphthalenes from 3-(2-alkynyl)aryl-¦Â-ketoesters
Satya Prakash Shukla, Rakesh Tiwari, Akhilesh Kumar Verma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


4 .     Tryptoquivaline J
C22H18N4O4     ÏàËÆ¶È:68.1%
Chemistry of Natural Compounds          2005          41          236-238
ALKALOIDS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus
Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


5 .     (1S,2S)-2-((3-fluorobenzyl)amino)-1,2,3,4-tetrahydronaphthalen-1-ol
C17H18NOF     ÏàËÆ¶È:64.7%
Organic Letters          2011          Vol.13,No.12          3000-3003
Diastereoselective Intramolecular Friedel-Crafts Alkylation of Tetralins
Cl¨¦mence Li¨¦bert, Marion K. Brinks, Andrew G. Capacci, Matthew J. Fleming, and Mark Lautens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


6 .     trans-(5S,6S)-4,5-dimethyl-2-(1-naphthyl)-6-phenyl-5,6-dihydro-4H-1,3,4-oxadiazine
C21H20N2O     ÏàËÆ¶È:64.7%
Journal of Heterocyclic Chemistry          2010          47          982-989
Synthesis and X-ray crystal structures of chiral, nonracemic 5,6-dihydro-4H-1,3,4-oxadiazines
Shawn R. Hitchcock, Melissa A. Dean, Christopher J. Kelley, Kate L. Edler and Gregory M. Ferrence
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


7 .     4-(4-fluorophenyl)-2-phenyl-1-p-tolyl-1H-imidazole
C22H17N2F     ÏàËÆ¶È:64.7%
Tetrahedron          2013          69          9417-9421
Iron(III)-catalyzed synthesis of multi-substituted imidazoles via [3+2] cycloaddition reaction of nitroolefins and N-aryl benzamidines Original Research Article
Xiang Liu, Dong Wang, Baohua Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


8 .     3-(4-Fluorophenyl)-4-(4-methylphenyl)-1-(4-nitrophenyl)-1H-pyrazole-5-carbonitrile
C23H15FN4O2     ÏàËÆ¶È:64.7%
Journal of the Brazilian Chemical Society          2009          20          975-987
Synthesis and Antimicrobial Evaluation of some New Pyrazole, Pyrazoline and Chromeno[3,4-c]pyrazole Derivatives
Nada M. Abunada, Hamdi M. Hassaneen, Ahmed S. M. Abu Samaha and Omar A. Miqdad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


9 .     ethyl 1-hydroxy-3-m-tolyl-2-naphthoate
C20H18O3     ÏàËÆ¶È:63.1%
Tetrahedron          2012          68          9035-9044
Silver-catalyzed regioselective synthesis of acridines, quinolines, and naphthalenes from 3-(2-alkynyl)aryl-¦Â-ketoesters
Satya Prakash Shukla, Rakesh Tiwari, Akhilesh Kumar Verma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


10 .     methyl 3-ethyl-2-hydroxy-6-methylthio-4-(b-naphthyl)-benzoate
C21H20O3S     ÏàËÆ¶È:61.9%
Tetrahedron          2013          69          5998-6007
Regioselective synthesis of 3-(methylthio)phenols by formal [3+3]-cyclocondensations of 3-oxo-bis(methylthio)ketenacetals with 1,3-bis(trimethylsilyloxy)-1,3-butadienes and 1,3-dicarbonyl dianions
Mathias Lubbe, Franziska Bendrath, Tiana Trabhardt, Alexander Villinger, Christine Fischer, Peter Langer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


11 .     methyl 1,2,3,10b-tetrahydro-3-(2-pyridyl)-pyrazolo[5,1-a]isoquinoline-1¦Á-carboxylate
C18H17N3O2     ÏàËÆ¶È:61.1%
Tetrahedron          1998          54          3735-3744
Isoquinolinium N-arylimides and electrophilic ethylenes: Structures and NMR spectra of cycloadducts
Helmut Huber, Rolf Huisgen, Kurt Polborn, David S. Stephenson, Robert Temme
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


12 .     anti-(Z)-(3-benzyl-5-ethoxycarbonylmethyl-1,4-dioxothiazolidin-2-ylidene)-N-phenylethanamide
C22H22N2O5S     ÏàËÆ¶È:61.1%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


13 .     ethyl 5-hydroxy-7-naphthalen-1-ylindane-4-carboxylate
C22H20O3     ÏàËÆ¶È:59.0%
Chemical & Pharmaceutical Bulletin          2013          61          768¨C775
One-Pot Synthesis of Phenol Derivatives by the Novel Intramolecular Alder¨CRickert Reaction: Effects of Aryl Substituent at the 3-Position of Cyclohexenone Derivatives on Reactivity
Atsushi Kinbara, Takehiro Yamagishi, Takeshi Fujishige, Hiroaki Miyaoka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


14 .     2-(4''-methoxybiphenyl-4'-yl)imidazo[2,1-b]benzothiazole
C22H16N2OS     ÏàËÆ¶È:58.8%
Bioorganic & Medicinal Chemistry          2011          19          1649-1657
Synthesis and biological evaluation of imidazolo[2,1-b]benzothiazole derivatives, as potential p53 inhibitors
Michael S. Christodoulou, Francesco Colombo, Daniele Passarella, Gabriella Ieronimo,Valentina Zuco, Michelandrea De Cesare, Franco Zunino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


15 .     N-{(Z/E)-1-{[(4-Fluorophenyl)amino]carbonyl}-2-[4-(dimethylamino) phenyl] vinyl} benzamide
C24H22FN3O2     ÏàËÆ¶È:58.8%
Archiv der Pharmazie          2011          11          292-300
Aminocarbonyl Arylvinylbenzamides as Gastric Sparing Anti-inflammatory Agents
Saurabh C. Khadse, Gokul S. Talele, and Surendra S. Agrawal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


16 .     methyl 1,2,3,4-tetrahydro-1-(2-chlorophenyl)-9H-pyrido[3,4-b]-indole-3-carboxylate
C19H17ClN2O2     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2006          43          767-772
Pictet-spengler cyclization in room temperature ionic liquid: A convenient access to tetrahydro ¦Â-carbolines
M. Muthukrishnan,Shivaji V. More,Dinesh R. Garud,C. V. Ramana,R. R. Joshi and R. A. Joshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


17 .     9b-hydroxy-5-methyl-3a-phenyl-3,3a,5,9b-tetrahydro-1H-imi-dazo[4,5-c]quinoline-2,4-dione
C17H15N3O3     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2006          43          1251-1260
Molecular rearrangement of 1-substituted 3-aminoquinoline-2,4-diones in their reaction with urea and nitrourea synthesis and transformations of reaction intermediates
Anton¨ªn Kl¨¢sek,Michal Kov¨¢ř,Ign¨¢c Hoza,Anton¨ªn Lyčka and Michal Holčapek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


18 .     Ethyl 2-(2,4-Dichlorophenylsulfonyl)-3-(2-chloroanilino)-acry- late
C17H14Cl3NO4S     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2005          42          1007-1010
A microwave induced cyclisation of-phenylsulfonyl-enaminoacrylates for the preparation of 4-aryl-4H-1,4-benzothiazine 1,1-dioxide derivatives
Sim¨®n E. L¨®pez,Jos¨¦ Salazar,Oscar Rebollo and Jelem Restrepo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


19 .     ethyl 2-N-1-Napthylamino-1,3-thiazole-5-carboxylate
C16H14N2O2S     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2003          40          353-356
Synthesis of novel 2-amino-1,3-thiazole-5-carboxylates utilising ultrasonic and thermally mediated aminolysis
Luke A. Baker and Craig M. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


20 .     1-phenyl-4,9-dihydro-3H-3,4-carbazoldione
     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2003          40          411-417
Synthesis and biological evaluation of structural variants of carbazoquinocin C
Alparslan Ayg¨¹n and Ulf Pindur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


21 .     1-(2-chlorophenyl)-1,2-dihydronaphtho[1,2-e][1,3] oxazin-3-one
C18H12ClNO2     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2010          47          313-317
An efficient one-pot three component synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-ones using montmorillonite K10 under solvent free conditions
Srinivas Kantevari, Srinivasu V. N. Vuppalapati, Rajashaker Bantu and Lingaiah Nagarapu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


22 .     compound 7g
C20H20ClFN4O3S     ÏàËÆ¶È:58.8%
Indian Journal of Chemistry Section B          2010          49B          923-928
Synthesis of 2-(4-substitutedsulfonyl piperazin-1-yl-methyl)-3-aryl-quinazolin-4(3H)-one
Palle V R Acharyulu,P K Dubey*,P V V Prasada Reddy & Thatipally Suresh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Óë¾ý³õÏàʶ£¬ÓÌÈç¹ÊÈ˹顣
2Â¥2013-12-05 15:10:23
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ Artclass µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 277Çóµ÷¼Á +3 Äß½¨Éè 2026-04-06 3/150 2026-04-06 22:39 by qlm5820
[¿¼ÑÐ] 304Çóµ÷¼Á +4 luoye0105 2026-04-05 4/200 2026-04-06 21:05 by ľ×Ó¾ý1218
[¿¼ÑÐ] Ò»Ö¾Ô¸¹ú¿Æ´óÐŹ¤Ëù,Ó¢¶þÊý¶þ408×Ü·Ö293·ÖÇóµ÷¼Á +3 ilcyuan 2026-04-02 4/200 2026-04-06 16:35 by likeihood
[¿¼ÑÐ] 320·ÖÈ˹¤ÖÇÄܵ÷¼Á +8 Õñ¡ªTZ 2026-04-03 8/400 2026-04-05 22:33 by ·¶Ê½Ë¼Î¬
[¿¼ÑÐ] 285Çóµ÷¼Á +4 ¶ñ·¨´ó¶þµÄÆøÎ¶ß 2026-04-05 5/250 2026-04-05 20:32 by 286640313
[¿¼ÑÐ] Çóµ÷¼ÁÇóµ÷¼Á +8 121. 2026-04-02 8/400 2026-04-05 20:15 by lys0704
[¿¼ÑÐ] 080200ѧ˶£¬277·Ö£¬ÊýÒ»104£¬Çó´ø×ߣ¡ +7 Æ¿×ÓPZ 2026-03-31 7/350 2026-04-05 17:49 by liucky
[¿¼ÑÐ] Ò»Ö¾Ô¸Î÷±±Å©ÁÖÐóÄÁר˶336·ÖÇóµ÷¼Á +3 5ourr 2026-04-03 3/150 2026-04-05 10:40 by JOKER0401
[¿¼ÑÐ] 320Çóµ÷¼Á +3 Ò»ÑùÔ² 2026-04-04 3/150 2026-04-04 22:29 by à£à£à£0119
[¿¼ÑÐ] 323Çóµ÷¼Á +8 Àî¼ÑÀÖ1 2026-04-04 8/400 2026-04-04 22:26 by hemengdong
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +18 Ò»ÑùYWY 2026-04-02 19/950 2026-04-04 22:14 by hemengdong
[¿¼ÑÐ] Ò»Ö¾Ô¸»ªÄÏʦ·¶361·Ö£¬»¯Ñ§Çóµ÷¼Á +7 Nicole88888 2026-04-01 7/350 2026-04-04 18:28 by macy2011
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +6 ·¶¸ùÅà 2026-04-04 6/300 2026-04-04 14:27 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] Ò»Ö¾Ô¸Î人Àí¹¤0856£¬³õÊÔ334 +3 26¿¼ÑвÄÁÏ 2026-04-02 3/150 2026-04-02 21:22 by dongzh2009
[¿¼ÑÐ] ÍÁľ304Çóµ÷¼Á +4 ÍÃͻͻͻ£¬ 2026-04-02 5/250 2026-04-02 21:16 by ÍÃͻͻͻ£¬
[¿¼ÑÐ] 275ѧ˶081000·þ´Óµ÷¼Áµ½ÆäËûרҵ£¬±£²»×¡±¾×¨ÒµÁË +7 һֻССˮţ 2026-04-02 8/400 2026-04-02 14:23 by alice-2022
[¿¼ÑÐ] Ò»Ö¾Ô¸9³õÊÔ366 ±¾Ë«·ÇÇóµ÷¼Á +4 ÔËÆøÀ´µÃÈôÓÐËÆÎ 2026-04-02 4/200 2026-04-02 09:56 by guanxin1001
[¿¼ÑÐ] 379Çóµ÷¼Á +3 ?¿à¹Ï²»¿à 2026-04-01 3/150 2026-04-01 20:09 by ÄºÔÆÇ庮
[¿¼ÑÐ] 353Çóµ÷¼Á +4 À­¹³²»Ðí±ä 2026-04-01 4/200 2026-04-01 18:10 by ¼Çʱ¾2026
[¿¼ÑÐ] ±¾2Ò»Ö¾Ô¸C9-333·Ö£¬²ÄÁÏ¿ÆÑ§Ó빤³Ì£¬Çóµ÷¼Á +9 ÉýÉý²»½µ 2026-03-31 9/450 2026-03-31 18:01 by Î޼ʵIJÝÔ­
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û