Diverse synthesis of pyrano[2,3-b]indol and dihydropyrano[2,3-b]indol via tunable Lewis bases catalyzed domino reactions

Tetrahedron

Volumn 71, Issue 40, 2015, Pages 7706-7716

  Liu, Yufen ^a   Du, Yanlong ^a   Yu, Aimin ^a   Qin, Dabin ^b   Meng, Xiangtai ^a  

^a TIANJIN UNIVERSITY OF TECHNOLOGY   (China)

^b CHINA WEST NORMAL UNIVERSITY   (China)

Author keywords

Allenoate chemistry; Diverse synthesis; Domino reactions; Lewis base catalysts; Tunable reactions

Indexed keywords

1,4 DIAZABICYCLO[2.2.2]OCTANE; 4 N,N DIMETHYLPYRIDINE; DIHYDROPYRANO[2,3 B]INDOL DERIVATIVE; ETHYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 CHLORO 4 (1,3 DIETHOXY 3 OXOPROP 1 EN 1 YL) 3,4 DIHYDROPYRANO[2,3 B]INDOL 9(2H)CARBOXYLATE; ETHYL 3 [9 ACETYL 2 (2 METHOXY 2 OXOETHYLIDENE) 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 CHLORO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 METHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 METHOXY 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 METHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 NITRO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 METHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 7 (TRIFLUOROMETHYL) 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYL] 4,9 DIHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [9 ACETYL 2 [2 (TERT BUTOXY) 2 OXOETHYLIDENE] 6 METHOXY 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 METHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 BROMO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 CHLORO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 FLUORO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 METHOXY 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6 METHYL 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 6,7 DIFLUORO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 7 BROMO 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; ETHYL 3 [ACETYL 2 [2 (BENZYLOXY) 2 OXOETHYLIDENE] 7 METHOXY 2,3,4,9 TETRAHYDROPYRANO[2,3 B]INDOL 4 YL] 3 ETHOXYACRYLATE; EXOCYCLIC DOUBLE BOND; INDOLE DERIVATIVE; LEWIS BASE; PYRAN DERIVATIVE; PYRANO[2,3 B]INDOL DERIVATIVE; REAGENT; TOLUENE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; ROOM TEMPERATURE;

EID: 84940595449     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2015.07.057     Document Type: Article

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