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2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-7-KETO-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE

Compound with spectra: 1 NMR

2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-7-KETO-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE
SpectraBase Compound ID 4V35IZ6AZQq
InChI InChI=1S/C31H33N3O5S/c1-31(2,3)39-30(36)27-20-33(18-23-16-24(35)15-22(17-32)29(23)27)14-13-21-19-34(28-12-8-7-11-26(21)28)40(37,38)25-9-5-4-6-10-25/h4-12,19-20,22-23,29H,13-16,18H2,1-3H3/t22-,23+,29+/m0/s1
InChIKey XYAQYKZFVBPUNJ-QFWOEDSFSA-N
Mol Weight 559.7 g/mol
Molecular Formula C31H33N3O5S
Exact Mass 559.214092 g/mol
Enantiomer InChIKey XYAQYKZFVBPUNJ-AFKLWXAFSA-N

View Spectrum of 2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-7-KETO-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-Isoquinolinecarboxylic acid, 5-cyano-1,2,4a,5,6,7,8,8a-octahydro-7-oxo-2-[2-[1-(phenylsulfonyl)-1H-indol-3-yl]ethyl]-, 1,1-dimethylethyl ester, (4a.alpha.,5.beta.,8a.alpha.)-(.+-.)-
2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-7-KETO-1,2,7,8,9,10-HEXAHYDROISOQUINOLINE
4-Isoquinolinecarboxylic acid, 1,2,4a,7,8,8a-hexahydro-7-oxo-2-[2-[1-(phenylsulfonyl)-1H-indol-3-yl]ethyl]-, 1,1-dimethylethyl ester, cis-(.+-.)-
1-Benzenesulfonyl-3-(6-butyl-2-thiophen-2-ylpyrimidin-4-yl)-1H-indole
1-[2-[1-(benzenesulfonyl)-2-(2-oxanyloxymethyl)-3-indolyl]ethyl]piperidine-2,3-dione
3-AZABICYCLO[3.3.1]NON-6-ENE, 4-[[1-[(4-METHOXYPHENYL)SULFONYL]-1H-INDOL-3-YL]METHYL]-2,2,6-TRIMETHYL-, (1R-ENDO)-
Methyl 4-((3-[(4,4,8-trimethyl-3-azabicyclo[3.3.1]non-7-en-2-yl)methyl]-1H-indol-1-yl)sulfonyl)phenyl ether
1,1'-Bis(benzenesulfonyl)-8-bromocoscinamide B
[(6R,8R)-1-(benzenesulfonyl)-6,8-dimethyl-7,8-dihydro-6H-cyclopenta[g]indol-5-yl]methanol
2-(4-{[4-methoxy-3-(6-methyl[1,2,4]triazolo[3,4-a]phthalazin-3-yl)phenyl]sulfonyl}-1-piperazinyl)ethanol
Title Journal or Book Year
Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systems Journal of the American Chemical Society 1990
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