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#8J;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY

Compound with spectra: 2 NMR

#8J;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY
SpectraBase Compound ID IYVg2keaNpG
InChI InChI=1S/C44H61NO5Si/c1-33(2)40(25-18-28-49-51(44(6,7)8,38-21-13-11-14-22-38)39-23-15-12-16-24-39)41(27-26-34-19-17-20-36(29-34)48-10)42(46)45-31-37(50-43(3,4)5)30-35(45)32-47-9/h11-17,19-24,26-27,29,35,37,40-41H,1,18,25,28,30-32H2,2-10H3/b27-26+/t35-,37+,40-,41+/m0/s1
InChIKey ASKXXCYGHXLAGR-DUWPVSMHSA-N
Mol Weight 712.1 g/mol
Molecular Formula C44H61NO5Si
Exact Mass 711.431901 g/mol
Enantiomer InChIKey ASKXXCYGHXLAGR-SRWVFECXSA-N

View Spectrum of #8J;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of #8J;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • #9J;ANTI-(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY
#9I;ANTI-(2S,3S)-1-[(2S,4R)-2-TERT.-BUTOXYMETHYL-4-METHOXY-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY
#8I;ANTI-(2R,3R)-1-[(2S,4R)-2-TERT.-BUTOXYMETHYL-4-METHOXY-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHY
#18J;ANTI-(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL
#17J;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL
#17K;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-TERT.-BUTOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-M
#18L;ANTI-(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-PHENOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL
#17I;ANTI-(2R,3R)-1-[(2S,4R)-2-TERT.-BUTOXYMETHYL-4-METHOXY-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL
#18I;ANTI-(2S,3S)-1-[(2S,4R)-2-TERT.-BUTOXYMETHYL-4-METHOXY-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL
4-{1'-[4"-(t-Butyldiphenylsilyl)oxy]butyl}-8,11,11-trimethyl-2-(phenymethoxy)bicyclo[5.3.1]undec-7-en-3-one
7'-(Ethoxycarbonyl)-2-[(t-butyldiphenylsilyl)oxymethyl]-1',2',3',6',9',9a'-hexahydrospiro[cyclopentane-1,4'-quinolizine
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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