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#16J;(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHYL-3-[3-(4-NITROPHENYL)-CARBONYLOXYPROPYL]-4-

Compound with spectra: 1 NMR

#16J;(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHYL-3-[3-(4-NITROPHENYL)-CARBONYLOXYPROPYL]-4-
SpectraBase Compound ID 4h6l4z5fUF2
InChI InChI=1S/C35H46N2O8/c1-24(2)31(12-9-19-44-34(39)26-14-16-27(17-15-26)37(40)41)32(18-13-25-10-8-11-29(20-25)43-7)33(38)36-22-30(45-35(3,4)5)21-28(36)23-42-6/h8,10-11,13-18,20,28,30-32H,1,9,12,19,21-23H2,2-7H3/b18-13+/t28-,30+,31+,32-/m0/s1
InChIKey CRBNSIWSBPAITB-GOCQBOKLSA-N
Mol Weight 622.8 g/mol
Molecular Formula C35H46N2O8
Exact Mass 622.325416 g/mol
Enantiomer InChIKey CRBNSIWSBPAITB-OLWQEIDSSA-N

View Spectrum of #16J;(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHYL-3-[3-(4-NITROPHENYL)-CARBONYLOXYPROPYL]-4-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#8E;ANTI-(2R,3R)-1-[(2S)-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-M
#17E;ANTI-(2R,3R)-1-[(2S)-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-ME
2,5-O-[BENZENE-1,2-DIYL-BIS-(OXYETHYLENEOXYETHYL)]-3,4-DI-O-DIBENZOYL-1,6-DIDEOXY-1,6-DIPHTHALIMIDO-D-MANNITOL
3(2H)-Indolizinone, hexahydro-6,7,8-tris(phenylmethoxy)-, [6R-(6.alpha.,7.alpha.,8.alpha.,8a.beta.)]-
(3S,4R,5S)-3,4-Dibenzyloxy-5-hydroxymethyl-N-(4-methoxybenzoyl)pyrrolidin-2-one
5-Methyl-2-[(4-methylphenyl)sulfonyl]-2,3-dihydro-1H-isoindol-4-yl 4-nitrobenzoate
6-BETA-BENZOYLOXY-3-ALPHA-(E)-(3,4,5-TRIMETHOXYCINNAMOYLOXY)-TROPANE-7-BETA-OL
2-(5,6-dibromo-1,3-dioxohexahydro-1H-4,7-methanoisoindol-2(3H)-yl)-4-methylpentanoic acid
(4R,5S)-3-[(2R,3S)-3-[(4-Nitrobenzoyl)oxy]-2-methyloctanoyl]-4-methyl-5-phenyl-2-oxazoidinone
(2E)-2-[4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-yl]-3-[(4-methyl-2-oxo-2H-chromen-7-yl)amino]-2-propenenitrile
Title Journal or Book Year
Zwitterionic Aza-Claisen Rearrangements Controlled by Pyrrolidine Auxiliaries - Useful Key Steps in Convergent Enantioselective Syntheses European Journal of Organic Chemistry 2012
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