For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

(3R,4R,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL

Compound with spectra: 1 NMR

(3R,4R,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL
SpectraBase Compound ID GcIlAh69eeb
InChI InChI=1S/C24H41NO4SSi/c1-12-20(22(26)16(2)3)21(15-29-31(10,11)24(7,8)9)25-30(27,28)23-18(5)13-17(4)14-19(23)6/h1,13-14,16,20-22,25-26H,15H2,2-11H3/t20-,21-,22-/m1/s1
InChIKey UMSMLYUGSFIUHD-YPAWHYETSA-N
Mol Weight 467.7 g/mol
Molecular Formula C24H41NO4SSi
Exact Mass 467.252557 g/mol
Enantiomer InChIKey UMSMLYUGSFIUHD-FKBYEOEOSA-N

View Spectrum of (3R,4R,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(3S,4S,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL
(3S,4S,5S)-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-6-PHENYLHEXAN-3-OL
(3R,4R,5S)-4-Ethynyl-2-methyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amono]-6-phenylhexan-3-ol
(3R,4R,5S)-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-6-PHENYLHEXAN-3-OL
Ethyl 3-methyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridin-2-carboxylate
N-1-{2-[(E)-N,N-Dimethylhydrazino]-1-ethylpentyl}-2,4,6-triisopropyl-1-benzenesulfonamide
N-cyclohexyl-2,4-dimethyl-3-[(methylsulfonyl)amino]benzenesulfonamide
3-(4-Methylphenyl)-3-[(2,4,5-trimethylphenyl)sulfonylamino]propanoic acid ethyl ester
N-[(R*)-{2-[(1R*,2S*)-2-(tert-Butyldimethylsilyloxymethyl)-4-oxocyclobutyl]-1-phenylethyl}-4-methylbenzenesulfonamide
N-[(3S)-4-[(tert-butyldimethylsilyl)oxy]-3-[[(4-methylphenyl)sulfonyl]amino]butyl]-N'-[(2R)-1-[(tert-butyldiphenylsilyl)oxy]-5-thiahex-2-yl]thiourea
Title Journal or Book Year
2-Ethynylaziridines as Chiral Carbon Nucleophiles:  Stereoselective Synthesis of 1,3-Amino Alcohols with Three Stereocenters via Allenylindium Reagents Bearing a Protected Amino Group The Journal of Organic Chemistry 2001
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.