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(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-6-PHENYL-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4(6H)-DIONE

Compound with spectra: 1 NMR

(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-6-PHENYL-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4(6H)-DIONE
SpectraBase Compound ID 2aj8cWeOhBA
InChI InChI=1S/C29H28N2O6/c1-34-23-11-10-17(13-24(23)35-2)12-21-29(33)31-22(28(32)30-21)14-19-15-25(36-3)26(37-4)16-20(19)27(31)18-8-6-5-7-9-18/h5-13,15-16,22,27H,14H2,1-4H3,(H,30,32)/b21-12-/t22-,27+/m0/s1
InChIKey NOZNNAVKRHBFLF-LBHNWOQZSA-N
Mol Weight 500.55 g/mol
Molecular Formula C29H28N2O6
Exact Mass 500.194737 g/mol
Enantiomer InChIKey NOZNNAVKRHBFLF-BSMKUVGCSA-N

View Spectrum of (+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-6-PHENYL-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4(6H)-DIONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-6-PROPYL-2,3,11,11A-TETRAHYDRO-6H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE
(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-6-ETHYL-8,9-DIMETHOXY-2,3,11,11A-TETRAHYDRO-6H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE
Dimethyl (3R,4S)-3-formyl-4-(nitromethyl)-1,2,3,4-tetrahydrocarbazole-1,1-dicarboxylate
Plucheaursenyl acetate [4,5-seco-18.beta.H-urs-20(30)en-3.beta.-yl acetate]
Spiro[2-(4-Methylphenylamino)-1,3-oxazolin-5-one-4,1'-imidazolo[2,3-a]isoquinoline]
10-Desmethoxy-10-N-cystino-dicholchamine
oxazolo[4,3-a]isoquinolin-3-one, 1-ethyl-1,5,6,10b-tetrahydro-8,9-dimethoxy-1,10b-dimethyl-
(R)-((1'S,4a'S,6'S,8a'S)-5',5',8a'-trimethyl-3',5-dioxo-3',4',4a',5',6',7',8',8a'-octahydro-2'H,5H-spiro[furan-2,1'-naphthalene]-6'-yl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
(S)-((1'S,4a'S,6'S,8a'S)-5',5',8a'-trimethyl-3',5-dioxo-3',4',4a',5',6',7',8',8a'-octahydro-2'H,5H-spiro[furan-2,1'-naphthalene]-6'-yl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
4,5,6,7-tetrachloro-2-methyl-3-(N'-phenylsuccinimido)isoindolin-1-one
Title Journal or Book Year
One-Pot α-Amidosulfone-Mediated Variation of the Pictet-Spengler Tetrahydroisoquinoline Synthesis, Suitable for Amide-Type Substrates European Journal of Organic Chemistry 2014
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