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Volumn 58, Issue 27, 2002, Pages 5407-5415
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Preparation of 3,4-enynoindoles via directed lithiation and application to the synthesis of 3,4-carbocycloindoles
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Author keywords
Cyclizations; Enynes; Indoles; Lithiation; Metathesis
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Indexed keywords
1 [3 DIMETHYLAMINOMETHYL 4 (1 HYDROXY 2 PROPENYL) 1 TRIISOPROPYLSILYL 1H INDOLE];
3 ALLYL 4 [1 (TERT BUTYLDIMETHYLSILANYLOXY)ALLYL] 1 TRIISOPROPYLSILANYL 1H INDOLE;
3 ALLYL 4 [1 (TERT BUTYLDIMETHYLSILYLOXY) 2 METHYLALLYL] 1 TRIISOPROPYLSILYL 1H INDOLE;
3 DIMETHYLAMINOMETHYL 4 (1 HYDROXY 2 METHYL 2 BUTENYL) 1 TRIISOPROPYLSILYL 1H INDOLE;
3 DIMETHYLAMINOMETHYL 4 (1 HYDROXY 2 METHYL 2 PROPENYL) 1 TRIISOPROPYLSILYL 1H INDOLE;
4 [1 (TERT BUTYLDIMETHYLSILYLOXY) 2 METHYLBUT 2 ENYL] 3 PROP 2 YNYL 1 TRIISOPROPYLSILYL 1H INDOLE;
6 (TERT BUTYLDIMETHYLSILYLOXY) 2 TRIISOPROPYLSILYL 6,9 DIHYDRO 2H 2 AZABENZO[CD]AZULENE;
6 (TERT BUTYLDIMETHYLSILYLOXY) 7 METHYL 2 TRIISOPROPYLSILYL 6,9 DIHYDRO 2H 2 AZABENZO[CD]AZULENE;
6 (TERT BUTYLDIMETHYLSILYLOXY) 7 METHYL 8 PROPENYL 2 TRIISOPROPYLSILYL 6,9 DIHYDRO 2H 2 AZABENZO[CD]AZULENE;
INDOLE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL MODIFICATION;
INFRARED SPECTROSCOPY;
LITHIATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS;
THIN LAYER CHROMATOGRAPHY;
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EID: 0036642530
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(02)00525-2 Document Type: Article |
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Times cited : (21)
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References (32)
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