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chzhbin½ð³æ (Ö°Òµ×÷¼Ò)
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| 32.82, 41.20, 55.27, 55.34, 55.62, 55.62, 71.88, 101.76, 103.89, 103.89, 110.19, 110.67, 120.42, 120.99, 121.70, 125.15, 126.50, 127.32, 127.37, 128.19, 128.43, 128.43, 128.79, 128.99, 131.57, 156.69, 157.06, 158.05, 158.05 |
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²éѯ½á¹û£º¹²²éµ½112¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-phenyl-1-(2,4-dimethoxyphenyl)benzo[1,8]naphthyridin-4(1H)-one C26H20N2O3 ÏàËÆ¶È:62.0% Tetrahedron 2013 69 2309-2318 Efficient synthesis of novel benzo[1,8]naphthyridin-4(1H)-ones and pyrido[2,3-b]quinoxalin-4(1H)-ones from alkynones and primary amines Viktor O. Iaroshenko, Muhammad Zahid, Satenik Mkrtchyan, Ashot Gevorgyan, Kai Altenburger, Ingo Knepper, Alexander Villinger, Vyacheslav Ya. Sosnovskikh, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-(2',6'-Dimethoxybenzoyl)-1,2-dihydroisoquinaldonitrile ÏàËÆ¶È:62.0% Tetrahedron 2012 68 8052-8067 The stereochemistry of isoquinoline Reissert compounds: a unique platform for observation of steric and electronic interactions Harry W. Gibson, Michael A.G. Berg, Terry L. Price Jr., Zhenbin Niu, Minjae Lee, Mason A. Rouser, Jennifer Clifton Dickson, Carla Slebodnick Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (E)-1,10-Dimethoxy-5a-phenyl-11-styryl-11a,12-dihydro-5aH,11H-chromeno[2,3-b]chromene C32H28O4 ÏàËÆ¶È:58.6% Bioorganic & Medicinal Chemistry 2012 20 1527-1534 Synthesis and antiplasmodial evaluation of novel chromeno[2,3-b]chromene derivatives Ruth Devakaram,David StC. Black,Vanida Choomuenwai,Rohan A. Davis,Naresh Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (E)-1,10-Dimethoxy-5a-(4-methoxyphenyl)-11-(4-methoxystyryl)-11a,12-dihydro-5aH,11H-chromeno[2,3-b]chromene C34H32O6 ÏàËÆ¶È:58.6% Bioorganic & Medicinal Chemistry 2012 20 1527-1534 Synthesis and antiplasmodial evaluation of novel chromeno[2,3-b]chromene derivatives Ruth Devakaram,David StC. Black,Vanida Choomuenwai,Rohan A. Davis,Naresh Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-(5-Benzyloxy-1H-indol-4-yl)-2-(4-benzyloxy-3-methoxyphenyl)-ethyl acetate C33H31NO5 ÏàËÆ¶È:58.6% Tetrahedron 2012 68 3708-3716 Synthetic studies of decursivine derivatives: preparation of key indole alkaloids via ¦Á-hydroxyalkylation Fumihiro Ito, Kentaro Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,2-bis(2-methoxyphenyl)naphthalene C24H20O2 ÏàËÆ¶È:58.6% Tetrahedron 2012 68 6305-6313 Synthesis of aryl-substituted naphthalenes by chemoselective Suzuki¨CMiyaura reactions of bromo-trifluoromethanesulfonyloxy-naphthalenes. Influence of steric and electronic parameters Zahid Hassan, Munawar Hussain, Alexander Villinger, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gliricidon C33H30O8 ÏàËÆ¶È:57.5% Journal of Natural Products 1999 62 188-190 New 12a-Hydroxyrotenoids from Gliricidia sepium Bark Luca Rastrelli, Ingeborg Berger, Wolfang Kubelka, Armando Caceres, Nunziatina De Tommasi, and Francesco De Simone Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-(2-Methoxyphenyl)-8-[(E)-(2-methoxyphenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine C32H29N3O4 ÏàËÆ¶È:56.6% Bioorganic & Medicinal Chemistry 2011 19 3444-3450 Antimycobacterial activity of novel 1,2,4-oxadiazole-pyranopyridine/chromene hybrids generated by chemoselective 1,3-dipolar cycloadditions of nitrile oxides Raju Ranjith Kumar,Subbu Perumal, J. Carlos Men¨¦ndez, Perumal Yogeeswari,Dharmarajan Sriram Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4 C34.5H33.5Cl8.5N2O4Si ÏàËÆ¶È:56.6% Zeitschrift f¨¹r Naturforschung B 2006 61 1406-1412 Syntheses of Allyl- and 3-Silylpropyl-substituted Salen-like Tetradentate Ligands via Hypercoordinate Silicon Complexes J. Wagler and G. Roewer Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N-[(1-benzyl-1H-indol-2-yl)methyl]-2,2,2-trichloro-N-(4-methoxybenzyl)acetamide C26H23Cl3N2O ÏàËÆ¶È:56.6% European Journal of Organic Chemistry 2010 5444-5453 Kharasch-Type Cyclizations of 2-Substituted Indole Derivatives Surprisingly Lead to Spiroindoles Sarah Van der Jeught, Nils De Vos, Kurt Masschelein, Ion Ghiviriga and Christian V. Stevens Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (E)-2,3-dihydro-5,6-dimethoxy-2-[(4-methoxyphenyl)methyl]-3-[(4-benzyloxy-2-bromophenyl)methylene]-1H-isoindol-1-one C32H28BrNO5 ÏàËÆ¶È:55.1% Natural Product Research 1999 13 33-40 An Expeditious Synthesis of Goniothalactam Axel Couture; Eric Deniau; Stephane Lebrun; Christophe Hoarau; Pierre Grandclaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . arundin trimethyl ether derivative C32H34O4 ÏàËÆ¶È:55.1% Phytochemistry 1993 32 439-444 Two stilbenoids from the orchid Arundina bambusifolia P. L. Majumder, Sabari Ghosal Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (E)-5a-(4-Chlorophenyl)-11-(4-chlorostyryl)-1,10-dimethoxy-11a,12-dihydro-5aH,11H-chromeno[2,3-b]chromene C32H26Cl2O4 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2012 20 1527-1534 Synthesis and antiplasmodial evaluation of novel chromeno[2,3-b]chromene derivatives Ruth Devakaram,David StC. Black,Vanida Choomuenwai,Rohan A. Davis,Naresh Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (E)-1,10-Dimethoxy-11-(4-methylstyryl)-5a-p-tolyl-11a,12-dihydro-5aH,11H-chromeno[2,3-b]chromene C34H32O4 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2012 20 1527-1534 Synthesis and antiplasmodial evaluation of novel chromeno[2,3-b]chromene derivatives Ruth Devakaram,David StC. Black,Vanida Choomuenwai,Rohan A. Davis,Naresh Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 11-[(o-chloro)phenyl]-8-[(o-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones C28H27ClN2O2S ÏàËÆ¶È:55.1% Journal of Heterocyclic Chemistry 2002 39 55-59 Synthesis and spectral properties of 11-[(o-; and p-substituted)-phenyl]-8-[(o-; m-;p-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1h-dibenzo[b,e][1,4]diazepin-1-ones Eduardo Cort¨¦as Cort¨¦as, Ana Mar¨ªa Hern¨¢ndez Sanabria and Olivia Garc¨ªa Mellado Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 11-[(p-chloro)phenyl]-8-[(o-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones C28H27ClN2O2S ÏàËÆ¶È:55.1% Journal of Heterocyclic Chemistry 2002 39 55-59 Synthesis and spectral properties of 11-[(o-; and p-substituted)-phenyl]-8-[(o-; m-;p-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1h-dibenzo[b,e][1,4]diazepin-1-ones Eduardo Cort¨¦as Cort¨¦as, Ana Mar¨ªa Hern¨¢ndez Sanabria and Olivia Garc¨ªa Mellado Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (E)-(3,4-Dimethoxyphenyl)(4-methoxy-2-((4-methoxybenzyl)oxy)-6-(4-methoxystyryl)phenyl)methanone C33H32O7 ÏàËÆ¶È:55.1% Molecules 2010 15 5909-5927 Modular Synthesis of Polyphenolic Benzofurans, and Application in the Total Synthesis of Malibatol A and Shoreaphenol David Y.-K. Chen, Qiang Kang and T. Robert Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 25 ÏàËÆ¶È:55.1% Tetrahedron Letters 2001 42 2493-2496 High-yielding TfOH-catalyzed condensation of phenols with aromatic aldehydes at high pressure. A model synthesis of the benzylidene biphenol key skeleton of blepharismins Takeshi Ohishi, Tomoyuki Kojima, Tatsuomi Matsuoka, Motoo Shiro, Hiyoshizo Kotsuki Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1,3-bis(2-methoxyphenyl)-9H-thioxanthen-9-one C27H20O3S ÏàËÆ¶È:55.1% Tetrahedron 2012 68 711-721 Suzuki¨CMiyaura reactions of the bis(triflates) of 1,3- and 1,4-dihydroxythioxanthone. Electronic and steric effects on the site-selectivity Dhafer Saber Zinad, Holger Feist, Alexander Villinger, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3-(4-Benzyloxy-3-methoxy-phenyl)-2-(5-benzyloxy-1H-indol-4-yl)-propionitrile C32H28N2O3 ÏàËÆ¶È:55.1% Tetrahedron 2012 68 3708-3716 Synthetic studies of decursivine derivatives: preparation of key indole alkaloids via ¦Á-hydroxyalkylation Fumihiro Ito, Kentaro Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 1-(5-Benzyloxy-1H-indol-4-yl)-2-(4-benzyloxy-3-methoxyphenyl)-ethanol C31H29NO4 ÏàËÆ¶È:55.1% Tetrahedron 2012 68 3708-3716 Synthetic studies of decursivine derivatives: preparation of key indole alkaloids via ¦Á-hydroxyalkylation Fumihiro Ito, Kentaro Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)quinoline-3-carboxamide C29H29N3O3 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-2-naphthamide C30H30N2O3 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 5-[(E/Z)-hydrazono(3,4,5-trimethoxyphenyl) methyl]-1-ethyl-1H-indole C20H23N3O3 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2008 16 5952-5961 Diarylmethyloxime and hydrazone derivatives with 5-indolyl moieties as potent inhibitors of tubulin polymerization Concepci¨®n ¨¢lvarez, Raquel ¨¢lvarez, Purificaci¨®n Corchete, Jos¨¦ Luis L¨®pez, Concepci¨®n P¨¦rez-Melero, Rafael Pel¨¢ez, Manuel Medarde Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 3c C24H22O4 ÏàËÆ¶È:55.1% European Journal of Organic Chemistry 2011 569-577 Lewis-Acid-Mediated Domino Reactions of Bis(diacetoxymethyl)-Substituted Arenes and Heteroarenes J. Arul Clement, Ramakrishnan Sivasakthikumaran, Arasambattu K. Mohanakrishnan, S. Sundaramoorthy and Devadasan Velmurugan Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . N-[(1-benzyl-1H-indol-2-yl)methyl]-2,2,2-trichloro-N-benzylacetamide C25H21Cl3N2O ÏàËÆ¶È:55.1% European Journal of Organic Chemistry 2010 5444-5453 Kharasch-Type Cyclizations of 2-Substituted Indole Derivatives Surprisingly Lead to Spiroindoles Sarah Van der Jeught, Nils De Vos, Kurt Masschelein, Ion Ghiviriga and Christian V. Stevens Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . cis-11-(diphenybnethyl)-N-[(2-methoxyphenyl)methyl]-1-azatricyclo[5.4.0.0(3,9)]undecan-10-amine C31H36N2O ÏàËÆ¶È:55.1% Journal of Medicinal Chemistry 1994 37 2831-2840 Aza-Tricyclic Substance P Antagonists John A. Lowe III, Susan E. Drozda, Stafford McLean, D. K. Bryce, Rosemary T. Crawford, R. Michael Snider, Kelly P. Longo, Atsushi Nagahisa, Megumi Tsuchiya Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 4k C28H26O4 ÏàËÆ¶È:55.1% Tetrahedron 2013 69 228-234 Synthesis of polyphenyls Meng-Yang Chang, Tein-Wei Lee, Shin-Ying Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 1-(3,4-dimethoxyphenyl)-2-phenylbenzo[1,8]naphthyridin-4(1H)-one C26H20N2O3 ÏàËÆ¶È:55.1% Tetrahedron 2013 69 2309-2318 Efficient synthesis of novel benzo[1,8]naphthyridin-4(1H)-ones and pyrido[2,3-b]quinoxalin-4(1H)-ones from alkynones and primary amines Viktor O. Iaroshenko, Muhammad Zahid, Satenik Mkrtchyan, Ashot Gevorgyan, Kai Altenburger, Ingo Knepper, Alexander Villinger, Vyacheslav Ya. Sosnovskikh, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1-(3,5-dimethoxyphenyl)-2-phenylbenzo[1,8]naphthyridin-4(1H)-one C26H20N2O3 ÏàËÆ¶È:55.1% Tetrahedron 2013 69 2309-2318 Efficient synthesis of novel benzo[1,8]naphthyridin-4(1H)-ones and pyrido[2,3-b]quinoxalin-4(1H)-ones from alkynones and primary amines Viktor O. Iaroshenko, Muhammad Zahid, Satenik Mkrtchyan, Ashot Gevorgyan, Kai Altenburger, Ingo Knepper, Alexander Villinger, Vyacheslav Ya. Sosnovskikh, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (R)-1-(1H-Indol-3-yl)-6,7-dimethoxy-3-phenyl-2-tosyl-1,2-dihydroisoquinoline C32H28N2O4S ÏàËÆ¶È:55.1% Tetrahedron 2012 68 5263-5268 Chiral counteranion-directed silver-catalyzed asymmetric synthesis of 1,2-dihydroisoquinolines by Friedel¨CCrafts alkylation reactions Jun-Wei Zhang, Zhe Xu, Qing Gu, Xiao-Xin Shi, Xue-Bing Leng, Shu-Li You Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (R)-3-Phenyl-1-(1-methyl-1H-indol-3-yl)-2-tosyl-1,2-dihydroisoquinoline C31H26N2O2S ÏàËÆ¶È:55.1% Tetrahedron 2012 68 5263-5268 Chiral counteranion-directed silver-catalyzed asymmetric synthesis of 1,2-dihydroisoquinolines by Friedel¨CCrafts alkylation reactions Jun-Wei Zhang, Zhe Xu, Qing Gu, Xiao-Xin Shi, Xue-Bing Leng, Shu-Li You Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . cis-(2,4-Dimethoxyphenyl)-4-(3,4-dimethoxyphenyl)-3-phenoxyazetidin-2-one C25H25NO6 ÏàËÆ¶È:55.1% Tetrahedron 2012 68 5505-5512 On-column N-dearylation of 2-azetidinones by silica-supported ceric ammonium nitrate Maaroof Zarei, Aliasghar Jarrahpour, Edris Ebrahimi, Malihe Aye, Seid Ali Torabi Badrabady Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (E)-8-(2-Methoxybenzylidene)-4-(2-methoxyphenyl)-3,4,5,6,7,8-hexahydropyrido[4,3-d]pyrimidine-2(1H)-thione C22H23N3O2S ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2013 23 3022-3031 Microwave assisted synthesis, cholinesterase enzymes inhibitory activities and molecular docking studies of new pyridopyrimidine derivatives Alireza, Basiri, Vikneswaran, Murugaiyah, Hasnah, Osman, Raju, Suresh, Kumar, Yalda, Kia, Mohamed, Ashraf, Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 4-benzoyl-3,5-bis(2-methoxyphenyl)-1,7-diphenylheptane-1,7-dione ÏàËÆ¶È:54.8% Helvetica Chimica Acta 2009 92 1102-1111 First Authentication of Kostanecki's Triketone and Multimolecular Reaction of Aromatic Aldehydes with Acetophenone Zixing Shan, Xiaoyun Hu, Lin Hu, Xitian Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 2,4-Bis[4-(9H-carbazol-9-yl)phenyl]-7-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine C49H33N5O ÏàËÆ¶È:54.8% Tetrahedron 2012 68 329-339 Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d]pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions Jelena Dodonova, Lina Skardziute, Karolis Kazlauskas, Saulius Jursenas, Sigitas Tumkevicius Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3-(N,N-Diisopropylamino)-1-(2-(1-methoxy)-3-phenyl-propyl)phenoxy)-2-propanol C25H37NO3 ÏàËÆ¶È:53.3% Archiv der Pharmazie 1998 331 233-240 A Combined Hansch/Free-Wilson Approach as Predictive Tool in QSAR Studies on Propafenone-Type Modulators of Multidrug Resistance Claudia Tmej, Peter Chiba, Mario Huber, Elisabeth Richter, Manuela Hitzler, Klaus-J¨¹rgen Schaper and Gerhard Ecker Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 2-(4-Methoxyphenyl)-5-(methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-¦Á-D-altropyranosid-3-yl-methyl)pyrazolo-[1,5-a]pyrimidine-3-carbonitrile C36H35N5O6 ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung B 2005 60 1175-1185 Synthesis of Iso-C-nucleoside Analogues from 1-(Methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-a-D- altropyranosid-3-yl)but-3-yn-2-ones I. Otero, H. Feist, D. Michalik, M. Michalik, J. Quincoces, and K. Peseke Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 2,4-Bis[4-(9H-carbazol-9-yl)phenyl]-7-phenyl-7H-pyrrolo [2,3-d]pyrimidine C48H31N5 ÏàËÆ¶È:53.3% Tetrahedron 2012 68 329-339 Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d]pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions Jelena Dodonova, Lina Skardziute, Karolis Kazlauskas, Saulius Jursenas, Sigitas Tumkevicius Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . compound 5e C34H30O4 ÏàËÆ¶È:53.3% Tetrahedron 2013 69 228-234 Synthesis of polyphenyls Meng-Yang Chang, Tein-Wei Lee, Shin-Ying Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . DO-19 ÏàËÆ¶È:53.1% Chemical & Pharmaceutical Bulletin 1990 38 2750-2755 Isoflavan and Related Compounds from Dalbergia odorifera. II Tetsu OGATA,Shoji YAHARA,Reiko HISATSUNE(nee SAIJO),Ryoji KONISHI and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . cis-N-[2-(3'',4''-dimethoxyphenyl)-9,10-dimethoxy-4-oxo-1-phenyl-3,4,6,7-tetrahydro-2H-pyrido[2,1-a]isoquinolin-3-yl]benzamide C36H34N2O6 ÏàËÆ¶È:53.1% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . Indolizine-1,2,3-triyltris((2-methoxyphenyl)methanone) C32H25NO6 ÏàËÆ¶È:53.1% Tetrahedron 2012 68 7338-7344 Convergent domino synthesis of 1,2,3-triaroylindolizines from methyl ketones and pyridines via self-division of labor strategy Yan Yang, Meng Gao, Dong-Xue Zhang, Liu-Ming Wu, Wen-Ming Shu, An-Xin Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 3-hydroxy-3-(hydroxy(2-methoxyphenyl)methyl)-2-methylisoindolin-1-one C17H17NO4 ÏàËÆ¶È:52.9% Tetrahedron 2012 68 8805-8816 Electroreductive intermolecular coupling of phthalimides with aldehydes: application to the synthesis of alkylideneisoindolin-1-ones Naoki Kise, Shinsaku Isemoto, Toshihiko Sakurai Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 7-hydroxy-2-(2-phenylethyl)chromone C17H14O3 ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2002 50(3) 419-422 Six New 2-(2-Phenylethyl)chromones from Agarwood Tenji KONISHI,Takao KONOSHIMA, Yasuo SHIMADA,and Shiu KIYOSAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . compound 1g ÏàËÆ¶È:51.7% Phytochemistry 1994 35 205-208 Two stilbenoids from the orchid arundina bambusifolia P.L. Majumder, Sabari Ghosal (N¨¦e Chatterjee) Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . arundin triacetate C35H34O7 ÏàËÆ¶È:51.7% Phytochemistry 1993 32 439-444 Two stilbenoids from the orchid Arundina bambusifolia P. L. Majumder, Sabari Ghosal Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 4-(Benzyloxy)-1-benzenesulfonyl-1'-(2,4-dimethoxybenzyl)-2,2'-bipyrrole C30H28N2O5S ÏàËÆ¶È:51.7% Canadian Journal of Chemistry 2008 86 213-218 Prodigiosin synthesis with electron rich 2,2'-bipyrroles Benoit Jolicoeur and William D. Lubell Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 3-benzoyl-4-(3,4-dimethoxyphenyl)-2-phenyl-5-(phenylsulfanyl-methyl)furan C32H26O4S ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2010 58 1180-1186 Scandium-Catalyzed Propargylation of 1,3-Diketones with Propargyl Alcohols Bearing Sulfur or Selenium Functional Groups: Useful Transformation to Furans and Pyrans Katsuki Ohta, Taira Kobayashi, Genzoh Tanabe, Osamu Muraoka and Mitsuhiro Yoshimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 11-[(o-methoxy)phenyl]-8-[(o-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones C29H30N2O3S ÏàËÆ¶È:51.7% Journal of Heterocyclic Chemistry 2002 39 55-59 Synthesis and spectral properties of 11-[(o-; and p-substituted)-phenyl]-8-[(o-; m-;p-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1h-dibenzo[b,e][1,4]diazepin-1-ones Eduardo Cort¨¦as Cort¨¦as, Ana Mar¨ªa Hern¨¢ndez Sanabria and Olivia Garc¨ªa Mellado Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 11-[(o-methoxy)phenyl]-8-[(m-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]-diazepin-1-ones C29H30N2O3S ÏàËÆ¶È:51.7% Journal of Heterocyclic Chemistry 2002 39 55-59 Synthesis and spectral properties of 11-[(o-; and p-substituted)-phenyl]-8-[(o-; m-;p-methoxy)phenylthio]-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1h-dibenzo[b,e][1,4]diazepin-1-ones Eduardo Cort¨¦as Cort¨¦as, Ana Mar¨ªa Hern¨¢ndez Sanabria and Olivia Garc¨ªa Mellado Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . 2-[2-(2,6-dichlorophenyl)amino]benzyl-3-{4-[5-(4-methoxy-phenyl)-1,3,4-oxadiazol-2-yl] phenyl}quinazolin-4(3H)one C36H25Cl2N5O3 ÏàËÆ¶È:51.7% Journal of Heterocyclic Chemistry 2010 47 923-931 Synthesis and antimicrobial activity of novel 1,3,4-oxadiazolyl-quinazolin-4(3H)ones Navin B. Patel and Jaymin C. Patel Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 5-[6-methoxy-2-(4-methoxyphenyl)-quinolin-4-yl]-2,3-diphenyl-3H-pyrimidin-4-one C33H25N3O3 ÏàËÆ¶È:51.7% Heterocycles 2010 80 379-393 Chemo- and Regioselective Imino Diels-Alder Reactions: Synthesis of Functionalized Novel Quinolin-3-one and Quinoline Derivatives Chander Mohan, Gaurav Bhargava, and Mohinder P. Mahajan Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . 5-[2-(4-chlorophenyl)-6-methoxy-quinolin-4-yl]-2-phenyl-3-p-tolyl-3H-pyrimidin-4-one C33H24ClN3O2 ÏàËÆ¶È:51.7% Heterocycles 2010 80 379-393 Chemo- and Regioselective Imino Diels-Alder Reactions: Synthesis of Functionalized Novel Quinolin-3-one and Quinoline Derivatives Chander Mohan, Gaurav Bhargava, and Mohinder P. Mahajan Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . (R)-2-(6-methoxy-1-(2-methoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)-1,1-diphenylethanol C31H31NO3 ÏàËÆ¶È:51.7% Heterocycles 2008 76 305-311 Synthesis of Chiral Tetrahydroisoquinoline-Derived ¦Â-Amino Alcohols and Their Application to Asymmetric Reaction Yoshiyuki Hari, Masaki Sakuma, Ayako Miyakawa, Keiichiro Hatano, and Toyohiko Aoyama Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . 3-Benzylsulfonyl-6-[4-(1-ethoxycarbonylethoxy)]phenoxy-5-(3-methylphenyl)-1-phenylpyrazolo[3,4-d]pyrimidin-4-one C36H32N4O7S ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry Letters 2007 17 2203-2209 Synthesis and herbicidal activity of novel pyrazolo[3,4-d]pyrimidin-4-one derivatives containing aryloxyphenoxypropionate moieties Hui Liu, Hong-Qing Wang, Zhao-Jie Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . compound 7a ÏàËÆ¶È:51.7% Tetrahedron Letters 2004 45 7469-7473 Synthesis of bioactive indolocarbazoles: synthesis, nucleophilic ring-opening and chiral base desymmetrisation of a cyclic sulfate intermediate Christopher J. Nichols, Nigel S. Simpkins Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound 11a ÏàËÆ¶È:51.7% Tetrahedron Letters 2005 46 7531-7534 1,5-Electrocyclisation of azomethine ylides leading to pyrrolo[2,1-a]isoquinolines¡ªconcise construction of the lamellarin skeleton Mikl¨®s Nyerges, L¨¢szl¨® Tőke Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . compound 1b ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 1996 4 1747-1753 Nitric oxide-induced oxidation of ¦Á-tocopherol Marco d'Ischia, Luisa Novellino Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . (3S)-7-((Naphtalen-1-yloxy)methyl)-5-oxo-8-(1-metyhyl-1H-indol-3-yl)-2,3-dihydro-5H-oxazolo[3,2-a]pyridine-3-carboxylic acid C28H20N2O5 ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2012 20 3128-3142 Mapping pilicide anti-virulence effect in Escherichia coli, a comprehensive structure¨Cactivity study Erik Chorell, Jerome S. Pinkner, Christoffer Bengtsson, Thomas Sainte-Luce Banchelin, Sofie Edvinsson, Anna Linusson, Scott J. Hultgren, Fredrik Almqvist Structure 13C NMR ̼Æ×Ä£Äâͼ |
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