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

Compound with spectra: 1 NMR

(3S,4S,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL
SpectraBase Compound ID JEW2Lt4nRJs
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-/m0/s1
InChIKey UMSMLYUGSFIUHD-BDTNDASRSA-N
Mol Weight 467.7 g/mol
Molecular Formula C24H41NO4SSi
Exact Mass 467.252557 g/mol
Enantiomer InChIKey UMSMLYUGSFIUHD-BHIFYINESA-N

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