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1- H-indole

Therapeutic Function Central stimulant Chemicel Name a-Ethyl-1 H-indole-3-ethanamine Common Name —... [Pg.614]

Chemical Name 3-(aminosulfonyl) 4-chloro-N-(2,3-dihydro-2-methyl-1 H-indol-Tyl)-benzamide... [Pg.807]

Chemical Name 1 -(4-Chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-1 H-indole-3-acetamide... [Pg.1124]

Representative procedure for conjugate reduction-aldol 3-CC 2- Hydroxy-[l-(toluene-4-sulfonyl)-1 H-indol-3-yl]-methyl -4,4-dimethylcyclohexanone [35]... [Pg.178]

TRYPTAMINE, 5-METHOXY-N,N-TETRAMETHYLENE INDOLE, 5-METHOXY-3-[2-(1-PYRROLIDYL)ETHYL] PYRROLIDINE, 1-[2-(5-METHOXY-1H-INDOL-3-YL)ETHYL] 5-METHOXY-N,N-TETRAMETHYLENETRYPTAMINE 5-METHOXY-3-[2-(1-PYRROLIDYL)ETHYL]INDOLE 1 -[2-(5-METHOXY-1 H-INDOL-3-YL)ETHYL]PYRROLIDINE "PYRROLIDYL-5-METHOXYTRYPTAMINE"... [Pg.214]

Chloro-benzoyl)-5-methoxy-2-methyl-1 H-indol-3-yl]-acetic acid carboxymethyl ester, C21H18CIN06, Mr 415,82, mp 150-153 °C (fine pale yellow crystals)... [Pg.43]

Nitromethane anion gives the corresponding N-allyl-3-(2-nitro-ethyl)- 2,3-dihydro-1-H-indole in 60% yield after photostimulated reaction with the bromide analogue, and in the presence of the enolate ion and acetone as an entrainment reagent (Scheme 10.51) [67]. [Pg.343]

INDOLES FROM 2-METHYLNITR0BEN2ENES BY CONDENSATION WITH FORMANIDE ACETALS FOLLOWED BY REDUCTION 4-BENZYLOXYINDOLE (1 H-Indole, 4-(phenylnethoxy) )... [Pg.214]

N -[2-( 1 H-Indol-3 -yl)ethyl] -N, dimethyl-1 -pyridin-2-yl cyclohexane-1,4-diamine Nonpolar 3HC1 ... [Pg.104]

DICHLORO-3-((1 E)-3-OXO-3-(PHEN YLAMINO)-1 -PROPENYL)-1 H-INDOLE-2-CARBOXYLIC ACID,... [Pg.466]

C8H1203 3-methyl-4-oxocyclohexanecarboxylic acid 101567-36-6 22.00 1.0630 2 14778 C8H15N octahydro-1 H-indole 4375-14-8 20.00 0.9472 1... [Pg.240]

C9H9N03 2,3-dihydro-3-hydroxy-1 -methyl-1 H-indole-5,6 54-06-8 25.00 1.2386 2 16580 C9H10N2O 4,5-dihydro-5-phenyl-2-oxazolamine 2207-50-3 25.00 1,1408 2... [Pg.244]

C11H120 1 -phenyl-1 -penten-3-one 3152-68-9 20.00 0.8697 1 22063 C11H14N20 5-methoxy-1 H-indole-3-ethanamine 608-07-1 25.00 1.0871 2... [Pg.257]

See other pages where 1- H-indole is mentioned: [Pg.268]    [Pg.1403]    [Pg.1866]    [Pg.2134]    [Pg.2206]    [Pg.1]    [Pg.455]    [Pg.30]    [Pg.282]    [Pg.260]    [Pg.1403]    [Pg.1404]    [Pg.1866]    [Pg.1866]    [Pg.2134]    [Pg.2206]    [Pg.225]    [Pg.294]    [Pg.512]    [Pg.2010]    [Pg.256]    [Pg.724]    [Pg.244]    [Pg.250]    [Pg.251]    [Pg.251]    [Pg.251]    [Pg.251]    [Pg.251]    [Pg.251]    [Pg.251]    [Pg.257]    [Pg.257]   
See also in sourсe #XX -- [ Pg.6 ]



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3-H-Indoles

3-H-Indoles

C—H borylation of indoles

C—H functionalization of indoles

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