Indexed keywords
14 ALLYL 5 METHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 BENZYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 ETHYL 5 METHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 ETHYL 5 PHENYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 ETHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 METHYL 5 PHENYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 METHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
14 PROP 2 YN 1 YL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
5 ETHYL 14 METHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
5,14 DIETHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
5,14 DIMETHYL 5,7,12,13 TETRAHYDRO 7,13 EPIMINO[2]BENZOTHIOCINO[3,4 B]INDOLE;
INDOLE DERIVATIVE;
ISOQUINOLINE DERIVATIVE;
PENTACYCLIC INDOYLTETRAHYDROISOQUINOLINE;
UNCLASSIFIED DRUG;
ACYLATION;
ALKYLATION;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL ANALYSIS;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
INTRAMOLECULAR C ALKYLATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS;
TANDEM S ALKYLATION;
3
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note
3)