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²éѯ½á¹û£º¹²²éµ½73¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ethyl 4-(4-methoxyphenyl)-3a,4-dihydro-3H,5H-[1,3]thiazolo[3'',4'':1',5']pyrrolo[2',3':3,4]pyrrolo[1,2-a]indole-4a(11bH)-carboxylate C25H26N2O3S ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¹³ÎǼî¼× ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2011 36 1305-1310 Chemical constituents of aerial parts ofGelsemium elegans ZHANG, Qiuping, ZHANG, Binfeng, CHOU, Guixin, WANG, Zhengtao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 9b C23H21N3O3 ÏàËÆ¶È:57.1% Journal of Heterocyclic Chemistry 2007 44 1373-1381 Stereochemistry of 1,3-dipolar-cycloaddition of 3,4-dihydroisoquinoline-and 3,4-dihydro-carboline-N-methoxycarbonyl-and N-phenacyl-methylides with maleic and fumaric nitrile Istv¨¢n K¨¢das,G¨¢bor Sz¨¢nt¨®,L¨¢szl¨® Tőke,Andr¨¢S Simon and G¨¢bor T¨®th Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ethyl 3-(4-chlorophenyl)-1-methyl-1,2,3,1'b-tetrahydropyrrolo[2',3':3,4]pyrrolo[1,2-a]indole-3a(4H)-carboxylate C23H23ClN2O2 ÏàËÆ¶È:57.1% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ethyl 4-(4-methoxyphenyl)-11-methyl-2,3,3a,4-tetrahydro-1H,5H-pyrrolizino[3',2':3,4]pyrrolo[1,2-a]indole-4a(11bH)-carboxylate C27H30N2O3 ÏàËÆ¶È:57.1% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . d-isocorydine-¦Â-N-oxide ÏàËÆ¶È:55% China Journal of Chinese Materia Medica 2009 34 2057-2059 Alkaloids from Dactylicapnos scandens Hutch WANG Fuhua, HU Xiao, CHEN Hailin, MA Jianping, WANG Jianxin, HOU Aijun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N-methylzenkerine ÏàËÆ¶È:55% Journal of Natural Products 1987 Vol 50 297 The 13C-Nmr Spectra of 1,2,10-Trioxygenated Aporphines Bruce K. Cassels, Andr¨¦ Cav¨¦, Michel Leboeuf Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 19-(R)-hydroxydihydrogelsemine C20H24N2O3 ÏàËÆ¶È:55% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 5 ÏàËÆ¶È:55% Heterocycles 2003 61 189-196 Two New Xenicane Diterpenoids from Okinawan Soft Coral of the Genus, Xenia Hiroaki Miyaoka, Masakazu Nakano, Kazuo Iguchi, and Yasuji Yamada* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 17 C19H27O4Br ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2011 19 7570-7581 Relevance of the C-5 position to schweinfurthin induced cytotoxicity Joseph J. Topczewski, Michael P. Callahan, John G. Kodet, Jery D. Inbarasu, Nolan R. Mente, John A. Beutler, David F. Wiemer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . pulcina ÏàËÆ¶È:55% Qu¨ªmica Nova 2007 30 92-98 Aporphine alkaloids in Ocotea species (Lauraceae) Zanin, Sandra Maria Warumby; Lordello, Ana Lu¨ªsa Lacava Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ethyl 1-methyl-3-phenyl-1,2,3,1'b-tetrahydropyrrolo[2',3':3,4]pyrrolo[1,2-a]indole-3a(4H)-carboxylate C23H24N2O2 ÏàËÆ¶È:55% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ethyl 4-phenyl-3a,4-dihydro-3H,5H-[1,3]thiazolo[3'',4'':1',5']pyrrolo[2',3':3,4]pyrrolo[1,2-a]indole-4a(11bH)-carboxylate C24H24N2O2S ÏàËÆ¶È:55% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 7(R),16(R),19(E)-isositsirikine oxindole C21H26N2O4 ÏàËÆ¶È:52.3% Phytochemistry 2009 70 1182-1186 Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana Kuan-Hon Lim, Kooi-Mow Sim, Guan-Huat Tan, Toh-Seok Kam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 19-(R)-hydroxydihydrogelsevirine C21H26N2O4 ÏàËÆ¶È:52.3% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 6b C23H21N3O3 ÏàËÆ¶È:52.3% Journal of Heterocyclic Chemistry 2007 44 1373-1381 Stereochemistry of 1,3-dipolar-cycloaddition of 3,4-dihydroisoquinoline-and 3,4-dihydro-carboline-N-methoxycarbonyl-and N-phenacyl-methylides with maleic and fumaric nitrile Istv¨¢n K¨¢das,G¨¢bor Sz¨¢nt¨®,L¨¢szl¨® Tőke,Andr¨¢S Simon and G¨¢bor T¨®th Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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