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TERT.-BUTYL-(3R,6R)-6-HEPT-6-ENYL-1-[(E)-[[(1S)-1-(METHOXYMETHYL)-2-METHYLPROPYL]-IMINO]-(PHENYL)-METHYL]-4-OXOPIPERIDIN-3-YLCARBAMATE

Compound with spectra: 1 NMR

TERT.-BUTYL-(3R,6R)-6-HEPT-6-ENYL-1-[(E)-[[(1S)-1-(METHOXYMETHYL)-2-METHYLPROPYL]-IMINO]-(PHENYL)-METHYL]-4-OXOPIPERIDIN-3-YLCARBAMATE
SpectraBase Compound ID C9y16lAVYM2
InChI InChI=1S/C30H47N3O4/c1-8-9-10-11-15-18-24-19-27(34)25(32-29(35)37-30(4,5)6)20-33(24)28(23-16-13-12-14-17-23)31-26(21-36-7)22(2)3/h8,12-14,16-17,22,24-26H,1,9-11,15,18-21H2,2-7H3,(H,32,35)/b31-28+/t24-,25-,26+/m1/s1
InChIKey XRZWFMDISKWTCJ-PSTZLPBVSA-N
Mol Weight 513.7 g/mol
Molecular Formula C30H47N3O4
Exact Mass 513.356657 g/mol
Enantiomer InChIKey XRZWFMDISKWTCJ-CNHWCKCJSA-N

View Spectrum of TERT.-BUTYL-(3R,6R)-6-HEPT-6-ENYL-1-[(E)-[[(1S)-1-(METHOXYMETHYL)-2-METHYLPROPYL]-IMINO]-(PHENYL)-METHYL]-4-OXOPIPERIDIN-3-YLCARBAMATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
TERT.-BUTYL-(6R)-6-ETHYL-1-[(E)-[[(1S)-1-(METHOXYMETHYL)-2-METHYLPROPYL]-IMINO]-(PHENYL)-METHYL]-4-OXO-1,4,5,6-TETRAHYDROPYRIDIN-3-YLCARBAMATE
(S)-1-CYCLOHEXYL-4-ISOPROPYL-2-(2-DIPHENYLPHOSPHANYL-PHENYL)-4,5-DIHYDROIMIDAZOLE
4H-Cyclohepta[d]pyrimidine-4-thione, 1-(2,2-dimethylpropyl)-1,5,6,7,8,9-hexahydro-2-phenyl-
2-METHYL-3-(2-OXO-3-PIPERIDINYL)QUINAZOLIN-4(3H)-ONE
2-Benzyl-6-exo-chloro-7-anti-phenylsulfenyl-2-aza-bicyclo(2.2.1)heptan-3-one
1-[(4ARS,8SR,8ASR)-4-BENZYL-8-(PYRROLIDIN-1-YL)-PERHYDRO-QUINOXALIN-1-YL]-2-(3,4-DICHLOROPHENYL)-ETHAN-1-ONE
((9S,10S)-9-Benzhydryl-8-aza-tricyclo[5.3.1.0*3,8*]undec-10-yl)-(2-trifluoromethyl-benzyl)-amine
(2R,3R,5R,6R)-2,6-DIBENZYLOXY-5-(TERT.-BUTYLDIMETHYLSILOXY)-3-(PARA-METHOXYBENZYLOXY)-4,4-DIMETHYL-7-OXOOCTANOL
3,6-dichloro-N-(2-oxo-2H-chromen-6-yl)-1-benzothiophene-2-carboxamide
Ambroxol-M (HO-) 4AC
Title Journal or Book Year
Stereoselective Synthesis of Pyridinones:  Application to the Synthesis of (−)-Barrenazines Organic Letters 2006
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