Indexed keywords
DIAZEPINE;
HETEROCYCLES;
HETEROCYCLIC COMPOUND;
ONE POT;
SYNTHESIS (CHEMICAL);
GOLD COMPOUNDS;
12,15B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
13 CYANO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
13 FLUORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
13 METHOXYL 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
13,15B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
13,16B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRIDO[2,1 C][1,4]DIAZEPINE 4,10(2H,16BH) DIONE;
14 METHOXYL 16B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRIDO[2,1 C][1,4]DIAZEPINE 4,10(2H,16BH) DIONE;
14,16B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRIDO[2,1 C][1,4]DIAZEPINE 4,10(2H,16BH) DIONE;
15,16B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRIDO[2,1 C][1,4]DIAZEPINE 4,10(2H,16BH) DIONE;
15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
16B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRIDO[2,1 C][1,4]DIAZEPINE 4,10(2H,16BH) DIONE;
2 HEXYL 13 FLUORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
2 HEXYL 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7 CHLORO 13 FLUORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7 CHLORO 13,15B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7 CHLORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7 FLUORO 13 CHLORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7 FLUORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7,13 DICHLORO 15B METHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7,13,15B TRIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7,15B DIMETHYL 13 CHLORO 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7,15B DIMETHYL 13 FLUORO 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
7,15B DIMETHYL 1H BENZO[E]INDOLO[1,2 A]PYRROLO[2,1 C][1,4]DIAZEPINE 3,9(2H,15BH) DIONE;
DIAZEPINE DERIVATIVE;
FUSED HETEROCYCLIC RINGS;
GOLD;
PYRROLO[2,1 C][1,4]BENZODIAZEPINE DERIVATIVE;
SILVER;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
CATALYST;
CHEMICAL REACTION;
ONE POT SYNTHESIS;
ANTIMONY;
AZEPINES;
CATALYSIS;
GOLD;
HETEROCYCLIC COMPOUNDS;
INDOLES;
MOLECULAR STRUCTURE;
PYRIDINES;
PYRROLES;
SILVER;
STEREOISOMERISM;
3
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CCDC 779689 contains the supplementary crystallographic data for 3Ba. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
CCDC 779689 contains the supplementary crystallographic data for 3Ba. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
45
79952147645
note
+ 396.1324, found 396.1327.
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note
To further explore the proposed mechanism, we treated 1B with the tautomer of intermediate A (α-angelica lactone, as shown below) under the optimized reaction conditions. Operational procedure: To a solution of α-angelica lactone (1.5 mmol) in dry toluene (3 mL) were added Au catalyst B (5 mol %) and AgSbF6 (20 mol%). After stirring at room temperature for 10 min, 1B (1 mmol) were added. Subsequently, the reaction vial was sealed, the mixture was heated to 120 °C for 12 h, and then, the cold mixture was concentrated under reduced pressure. The resulting residue was purified by flash column chromatography to afford 3Ba in 90% yield.