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2-(N-TERT.-BUTOXYCARBONYLALLYL)-4-(TERT.-BUTOXYCARBONYL)-7-KETO-1,2,7,8,9,10-HEXAHYDROISOQUINOLINE

Compound with spectra: 1 NMR

2-(N-TERT.-BUTOXYCARBONYLALLYL)-4-(TERT.-BUTOXYCARBONYL)-7-KETO-1,2,7,8,9,10-HEXAHYDROISOQUINOLINE
SpectraBase Compound ID LRqT4vzmT9S
InChI InChI=1S/C31H38N2O5/c1-30(2,3)37-28(35)14-16-33-19-21(25-9-7-8-10-27(25)33)13-15-32-18-22-17-23(34)11-12-24(22)26(20-32)29(36)38-31(4,5)6/h7-12,14,16,19-20,22,24H,13,15,17-18H2,1-6H3/b16-14+/t22-,24-/m1/s1
InChIKey PXOCPHKPSUDNIS-ZPSHTPPSSA-N
Mol Weight 518.7 g/mol
Molecular Formula C31H38N2O5
Exact Mass 518.278072 g/mol
Enantiomer InChIKey PXOCPHKPSUDNIS-OIHOTYHGSA-N

View Spectrum of 2-(N-TERT.-BUTOXYCARBONYLALLYL)-4-(TERT.-BUTOXYCARBONYL)-7-KETO-1,2,7,8,9,10-HEXAHYDROISOQUINOLINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-Isoquinolinecarboxylic acid, 2-[2-[1-[3-(1,1-dimethylethoxy)-3-oxo-1-propenyl]-1H-indol-3-yl]ethyl]-1,2,4a,7,8,8a-hexahydro-7-oxo-, 1,1-dimethylethyl ester, [2(E),4a.alpha.,8a.alpha.]-(.+-.)-
.delta.3,.delta.5-2-Tryptophyl-4-carbethoxy-7-[1,1-(ethylenedioxy)-ethyl]hexahydroisoquinoline
8-[N-(PHENYLSULFONYL)-TRYPTOPHYL]-8-AZA-4-ACETYL-4-HYDROXYBICYCLO-[4.2.0]-OCT-2-ENE
DELTA(4A,10B),DELTA(8)-2,5-DIMETHYL-8-[1,1-(ETHYLENEDIOXY)-ETH-1-YL]-1-OXO-DECAHYDRO-PHENANTHRIDINE
5MT-NB3OMe 2PFP
Azonino[5,4-b]indole-7-carboxylic acid, 1,2,3,4,5,6,7,8-octahydro-5-[3-[[(4-methylphenyl)sulfonyl]oxy]propyl]-3-(phenylmethyl)-, methyl ester, (5R*,7R*)-(.+-.)-
TRANS-3-(METHOXYCARBONYL)-N(A)-METHYL-1-METHYL-1,2,3,4-TETRAHYDRO-BETA-CARBOLINE
CIS-3-(METHOXYCARBONYL)-N(A)-METHYL-1-METHYL-1,2,3,4-TETRAHYDRO-BETA-CARBOLINE
2H-3,7-Methanoazacycloundecino[5,4-b]indole-9-carboxylic acid, 5-ethyl-1,4,7,8,9,10-hexahydro-, methyl ester, [7R-(7R*,9R*)]-
(5S,7R)-3-benzyl-5-[(1R)-1-hydroxyethyl]-2,4,5,6,7,8-hexahydro-1H-azonin[5,4-b]indole-7-carboxylic acid methyl ester
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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