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Volumn 68, Issue 19, 2012, Pages 3708-3716
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Synthetic studies of decursivine derivatives: Preparation of key indole alkaloids via α-hydroxyalkylation
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Author keywords
Indole alkaloid; ortho Selective hydroxyalkylation; Uhle's ketone
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Indexed keywords
(4 BENZYLOXY 3 METHOXY PHENYL)ACETALDEHYDE;
1 (5 BENZYLOXY 1H INDOL 4 YL) 2 (4 BENZYLOXY 3 METHOXY PHENYL)ETHANOL;
1 (5 BENZYLOXY 1H INDOL 4 YL) 2 (4 BENZYLOXY 3 METHOXY PHENYL)ETHANONE;
1 (5 BENZYLOXY 1H INDOL 4 YL) 2 (4 BENZYLOXY 3 METHOXY PHENYL)ETHYL ACETATE;
1 [5 BENZYLOXY 3 (2 HYDROXY ACETYL) 1H INDOL 4 YL] 2 (4 BENZYLOXY 3 METHOXY PHENYL)ETHANONE;
1 BENZYL 6 BENZYLOXY 5 (4 BENZYLOXY 3 METHOXY BENZYL) 4 HYDROXY 1H BENZO[CD]INDOLE 3 ONE;
2 (4 BENZYLOXY 3 METHOXY PHENYL) 1 [5 BENZYLOXY 1 (TOLUENE 4 SULFONYL) 1H INDOL 4 YL]ETHANOL;
2 (4 BENZYLOXY 3 METHOXY PHENYL) 1 [5 BENZYLOXY 1 (TOLUENE 4 SULFONYL) 1H INDOL 4 YL]ETHANONE;
2 (4 BENZYLOXY 3 METHOXY PHENYL) 1 [5 BENZYLOXY 1 (TOLUENE 4 SULFONYL) 1H INDOL 4 YL]ETHYL ACETATE;
2 (4 BENZYLOXY 3 METHOXY PHENYL) 1 [5 BENZYLOXY 1 (TOLUENE 4 SULFONYL) 1H INDOL 4 YL]PROPIONITRILE;
2 [5 BENZYLOXY 4 [2 (4 BENZYLOXY 3 METHOXY PHENYL)ACETYL] 1 (TOLUENE 4 SULFONYL) 1H INDOL 3 YL] 2 OXO ETHYL ACETATE;
2 [5 BENZYLOXY 4 [2 (4 BENZYLOXY 3 METHOXY PHENYL)ACETYL] 1 BENZYL 1H INDOL 3 YL] 2 OXO ETHYL ACETATE;
2 [5 BENZYLOXY 4 [2 (4 BENZYLOXY 3 METHOXY PHENYL)ACETYL] 1H INDOL 3 YL] 2 OXO ETHYL ACETATE;
3 (4 BENZYLOXY 3 METHOXY PHENYL) 2 (5 BENZYLOXY 1H INDOL 4 YL)PROPIONITRILE;
3 (4 BENZYLOXY 3 METHOXYPHENYL) 2 HYDROXYACRYLIC ACID;
3 (4 BENZYLOXY 3 METHOXYPHENYL) 2 HYDROXYACRYLIC ACID METHYL ESTER;
4 [2 (4 BENZYLOXY 3 METHOXY PHENYL) 1 HYDROXY ETHYL] 1 (TOLUENE 4 SULFONYL) 1H INDOL 5 OL;
5 (4 BENZYLOXY 3 METHOXYBENZYLIDEN)IMIDAZOLIDINE 2,4 DIONE;
6 BENZYLOXY 4 (4 BENZYLOXY 3 METHOXY PHENYL) 5 OXO 1,5 DIHYDRO BENZO[CD]INDOLE 3 CARBOXYLIC ACID BENZYLAMIDE;
6 BENZYLOXY 4 (4 BENZYLOXY 3 METHOXY PHENYL) 5 OXO 1,5 DIHYDRO BENZO[CD]INDOLE 3 CARBOXYLIC ACID METHYL ESTER;
[5 BENZYLOXY 3 (2 HYDROXY ACETYL) 1 BENZYL 1H INDOL 4 YL] 2 (4 BENZYLOXY 3 METHOXY PHENYL)ETHANONE;
[5 BENZYLOXY 4 [2 (4 BENZYLOXY 3 METHOXY PHENYL)ACETYL] 1H INDOL 3 YL] OXO ACETIC ACID METHYL ESTER;
DECURSIVINE;
DECURSIVINE DERIVATIVE;
FLAVUMINDOLE;
INDOLE ALKALOID;
MOSCHAMININDOLOL;
N BENZYL 2 [5 BENZYLOXY 4 [2 (4 BENZYLOXY 3 METHOXY PHENYL)ACETYL] 1H INDOL 3 YL] 2 OXO ACETAMIDE;
SEROTOBENINE;
TRIBUTYLTIN CHLORIDE;
UNCLASSIFIED DRUG;
ALKYLATION;
ALPHA HYDROXYALKYLATION;
ARTICLE;
CHEMICAL MODIFICATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
PRIORITY JOURNAL;
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EID: 84859570864
PISSN: 00404020
EISSN: 14645416
Source Type: Journal
DOI: 10.1016/j.tet.2012.03.026 Document Type: Article |
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Times cited : (7)
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References (32)
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