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(2S,4R)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY-2-METHYLHEX-2-ENYL]-4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

Compound with spectra: 1 NMR

(2S,4R)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY-2-METHYLHEX-2-ENYL]-4-HYDROXYPYRROLIDINE-2-CARBOXYLATE
SpectraBase Compound ID NiZ0pYwqir
InChI InChI=1S/C29H41NO4Si/c1-23(21-30-22-24(31)20-27(30)28(32)33-5)14-12-13-19-34-35(29(2,3)4,25-15-8-6-9-16-25)26-17-10-7-11-18-26/h6-11,14-18,24,27,31H,12-13,19-22H2,1-5H3/b23-14+/t24-,27+/m1/s1
InChIKey VTQQBGBAIKBIBC-HTXMEQGCSA-N
Mol Weight 495.7 g/mol
Molecular Formula C29H41NO4Si
Exact Mass 495.280485 g/mol
Enantiomer InChIKey VTQQBGBAIKBIBC-SJTZTZPTSA-N

View Spectrum of (2S,4R)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY-2-METHYLHEX-2-ENYL]-4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTOXYMETHYL)-4-METHOXYPYRROLIDINE
RJBIWSAVZGAIBV-YSEONISGSA-N
(2S,9R,10S)-9-(5-(TERT.-BUTYLDIPHENYLSILYLOXY)-PENTYL)-2-(HYDROXYMETHYL)-1-OXAQUINOLIZIDINE;HYDROCHLORIDE-SALT
Ethyl 4(S)-7-((tert-Butyldiphenylsilyl)oxy)-4-[1(S)-1-(4(R)-2,2-dimethyl[1,3]dioxolan-4-yl]propoxy]heptanoate
5-[7-(t-Butyldiphenylsilyloxy)-3-methylhept-2-enyl]furo[2,3-b]pyridine
[(2R,3S,6R)-6-[3-[tert-butyl(diphenyl)silyl]oxypropyl]-3-hydroxy-tetrahydropyran-2-yl]methyl 4-methylbenzenesulfonate
(4R*,5R*)-2,2,5-Trimethyl-4-[4-(tert-butyldiphenylsilyloxy)butyl]-4-methoxymethyl-1,3-dioxolane
(2S)-2-(tert-Butyldiphenylsilyloxymethyl)-1-azabicyclo[2.2.2]octan-5-ol
7-tert-Butyldiphenylsilyloxy-2-diphenylphosphinoylheptan-3-one
(2S)-2-[(tert-Butyldiphenylsilyloxy)methyl]-1-(benzyloxycarbonyl)-4-pyrroline
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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