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(2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANOL-MOSHER-ACID

Compound with spectra: 1 NMR

(2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANOL-MOSHER-ACID
SpectraBase Compound ID 9HZhTtUYGsY
InChI InChI=1S/2C30H44F3NO5Si2/c2*1-28(2,3)41(8,9)39-21-25(34(22-40(5,6)7)26(35)23-16-12-10-13-17-23)20-38-27(36)29(37-4,30(31,32)33)24-18-14-11-15-19-24/h2*10-19,25H,20-22H2,1-9H3/t25-,29+;25-,29-/m00/s1
InChIKey OTNHQVXAAYTMAI-HNIUMNNYSA-N
Mol Weight 1223.7 g/mol
Molecular Formula C60H88F6N2O10Si4
Exact Mass 1222.542022 g/mol
Enantiomer InChIKey OTNHQVXAAYTMAI-DQXCUVTPSA-N

View Spectrum of (2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANOL-MOSHER-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S)-3-(tert-Butyldimethylsiloxy)-2-[N-[(trimethylsilyl)methyl]-N-benzoylamino]-1-propanol methoxy(trifluoromethyl)phenylacetic acid ester
3,3,3-TRIFLUORO-2-METHOXY-2-PHENYL-PROPIONIC-ACID-4-ACETYL-INDAN-2-YL-ESTER
(R)-2,2-Bis(prop-2-yn-1-yl)cyclohexanone-3-MTPA ester
(S)-((R)-1-cyclohexenyl-3,3-dimethoxy-1-oxopropan-2-yl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
[(1S)-1-(2-oxo-6,8a-dihydro-4aH-pyrano[3,2-b]pyran-6-yl)ethyl] (2S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propanoate
DIETHYL-[1,1-DIFLUORO-3-(3-S)-[(S)-ALPHA-METHOXY-ALPHA-(TRIFLUOROMETHYL)-PHENYLACETYL]-4-(OLEOYLOXY)-BUTYL]-PHOSPHONATE
DIETHYL-[1,1-DIFLUORO-3-(3-R)-[(S)-ALPHA-METHOXY-ALPHA-(TRIFLUOROMETHYL)-PHENYLACETYL]-4-(OLEOYLOXY)-BUTYL]-PHOSPHONATE
(S)-((R)-1-(3,5-dimethoxyphenyl)-3-methyl-1-oxobut-3-en-2-yl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
(2R)-1-[(2S)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]-1-pyrrolidinyl]-3,3,3-trifluoro-2-methoxy-2-phenyl-1-propanone
(S)-2-Pyrrolidinemethanol tert-Butyldimethylsilyl Ether (S)-MTPA-amide
Title Journal or Book Year
An Oxidative Mannich Cyclization Methodology for the Stereocontrolled Synthesis of Highly Functionalized Piperidines The Journal of Organic Chemistry 1998
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