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#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

Compound with spectra: 1 NMR

#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
SpectraBase Compound ID 2huJSbbgPBk
InChI InChI=1S/C47H69NO5Si/c1-35(2)42(27-20-30-52-54(47(9,10)11,40-23-15-13-16-24-40)41-25-17-14-18-26-41)43(29-28-36-21-19-22-38(31-36)50-12)44(49)48-33-39(53-46(6,7)8)32-37(48)34-51-45(3,4)5/h13-19,21-26,31,37,39,42-43H,1,20,27-30,32-34H2,2-12H3/t37-,39+,42-,43+/m0/s1
InChIKey OHPQTYFBBJRRII-SEJARBKDSA-N
Mol Weight 756.2 g/mol
Molecular Formula C47H69NO5Si
Exact Mass 755.494501 g/mol
Enantiomer InChIKey OHPQTYFBBJRRII-UCLDCFMGSA-N

View Spectrum of #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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#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
#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
#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
#8K;ANTI-(2R,3R)-1-[(2S,4R)-4-TERT.-BUTOXY-2-TERT.-BUTOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-
#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
#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
4-{1'-[4"-(t-Butyldiphenylsilyl)oxy]butyl}-8,11,11-trimethyl-2-(phenymethoxy)bicyclo[5.3.1]undec-7-en-3-one
(2S,3R,4E)-1-[(TERT.-BUTYL)-DIPHENYLSILYLOXY]-16-METHYL-2-(21-METHYLDOCOSANAMIDO)-HEXADEC-4-EN-3-YL-(S)-3,3,3-TRIFLUORO-2-METHOXY-2-PHENYLPROPANOATE
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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