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#12G;ANTI-(2R,3R)-2-[(E)-2-(2-BROMO-5-METHOXYPHENYL)-ETHENYL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,4R)-2-(METHOXYMETHOXYMETHYL)-4-METHOXYMETHYLOXY-PY

Compound with spectra: 1 NMR

#12G;ANTI-(2R,3R)-2-[(E)-2-(2-BROMO-5-METHOXYPHENYL)-ETHENYL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,4R)-2-(METHOXYMETHOXYMETHYL)-4-METHOXYMETHYLOXY-PY
SpectraBase Compound ID 55ltHhZATMy
InChI InChI=1S/C43H58BrNO7Si/c1-32(2)39(20-15-25-52-53(43(3,4)5,37-16-11-9-12-17-37)38-18-13-10-14-19-38)40(23-21-33-26-35(49-8)22-24-41(33)44)42(46)45-28-36(51-31-48-7)27-34(45)29-50-30-47-6/h9-14,16-19,21-24,26,34,36,39-40H,1,15,20,25,27-31H2,2-8H3/b23-21+/t34-,36+,39+,40+/m0/s1
InChIKey VXRRZLBRHJBYLL-PIIGKMMNSA-N
Mol Weight 808.9 g/mol
Molecular Formula C43H58BrNO7Si
Exact Mass 807.316593 g/mol
Enantiomer InChIKey VXRRZLBRHJBYLL-DRNZPXCPSA-N

View Spectrum of #12G;ANTI-(2R,3R)-2-[(E)-2-(2-BROMO-5-METHOXYPHENYL)-ETHENYL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,4R)-2-(METHOXYMETHOXYMETHYL)-4-METHOXYMETHYLOXY-PY

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#13G;ANTI-(2S,3S)-2-[(E)-2-(2-BROMO-5-METHOXYPHENYL)-ETHENYL]-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,4R)-2-(METHOXYMETHOXYMETHYL)-4-METHOXYMETHYLOXY-PY
tert-Butyl-[2-[2-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-3-yl)-4,5-dimethoxy-phenyl]ethoxy]-diphenyl-silane
2-[(1S,3S)-1-[2-[tert-butyl(diphenyl)silyl]oxyethyl]-2,3,4,9-tetrahydro-1H-$b-carbolin-3-yl]acetonitrile
N-[1-[2-[2-[(tert-butyldiphenylsilyl)oxy]ethyl]-4,5-dimethoxyphenyl]-2-(3,4-dimetjoxyphenyl)ethyl]benzamide
2-Amino-9-[5-O-(tert-Butyldiphenylsilyl)-2,3-dideoxy-.beta.,D-glycero-penta-2-enofuranosyl]-6-methoxypurine
ETHYL-3-(4'-TERT.-BUTYLDIPHENYLSILYLOXYMETHYL-1'-METHYLINDOL-3'-YL)-3-OXOPROPANOATE;OXO-TAUTOMER
N(1)-[(5''-ACETOXYETHOXY)-METHYL]-N(9)-[(5'-TERT.-BUTYLDIPHENYLSILYLOXYETHOXY)-METHYL]-8-TRIFLUOROMETHYL-HYPOXANTHINE
ethyl 5-(3,4-dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate
2'-[1"-(Benzyloxy)-3"-hydroxyprop-2"-yl]-2-[(t-butyldiphenylsilyl)oxymethyl]-hexahydrospiro[cyclopentane-1,7'-isoxazolo[2,3-a]pyridine
2.beta.-Methyl-19-nor-1.alpha.,25-dihydroxyvitamin D3 - 3-[(t-butyl)diphenylsilyl] - derivative
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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