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[3S,4S,5S,6R]-N-BENZYLOXYCARBONYL-3,4,5,6-TETRAHYDRO-4,5-DIHYDROXY-3-METHYL-6-(PARA-TOLYLSULFONYL)-1,2-OXAZINE

Compound with spectra: 1 NMR

[3S,4S,5S,6R]-N-BENZYLOXYCARBONYL-3,4,5,6-TETRAHYDRO-4,5-DIHYDROXY-3-METHYL-6-(PARA-TOLYLSULFONYL)-1,2-OXAZINE
SpectraBase Compound ID 16cKNoAeJaJ
InChI InChI=1S/C20H23NO6S/c1-13-8-10-16(11-9-13)28(25)19-18(23)17(22)14(2)21(27-19)20(24)26-12-15-6-4-3-5-7-15/h3-11,14,17-19,22-23H,12H2,1-2H3/t14-,17-,18-,19+,28?/m0/s1
InChIKey AJASFZNTYPDNNO-BXRCMHNLSA-N
Mol Weight 405.47 g/mol
Molecular Formula C20H23NO6S
Exact Mass 405.124609 g/mol
Enantiomer InChIKey AJASFZNTYPDNNO-JGHZXGEMSA-N

View Spectrum of [3S,4S,5S,6R]-N-BENZYLOXYCARBONYL-3,4,5,6-TETRAHYDRO-4,5-DIHYDROXY-3-METHYL-6-(PARA-TOLYLSULFONYL)-1,2-OXAZINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2'S,4S,5S)-2,2-Dimethyl-5-[(tert-butyldimethylsilyloxy)methyl]-4-[2'-[(4"-methylphenyl)thio]-1'-[(tert-butyloxycarbonyl)amino]-2'-oxoethyl]-1,3-dioxolane
(2'R,4S,5S)-2,2-Dimethyl-5-[(tert-butyldimethylsilyloxy)methyl]-4-[2'-(4"-methylphenyl)thio]-1'-[(tert-butyloxycarbonyl)amino]-2'-oxoethyl]-1,3-dioxolane
(1R,4S,6S,7S)-2-Oxa-3-methyl-5-azabicyclo[4.1.0]heptane-4,5,7-tricarboxylic acid - 5-Benzyl ester,4-Methyl ester
(2S,3S,4R,5R)-1-[(tert-butyldimethylsilyl)oxy]-2,3-(isopropylidenedioxy)-5-[[[p-(methoxybenzyl)oxy]carbonyl]amino]-4,6-bis(methoxymethoxy)hexane
1-DEOXY-1-(p-TOLYLSULFINYL)-beta-D-XYLOSE, TRIACETATE
METHYL-3,4,6-TRI-O-BENZYL-2-DEOXY-2-(2,2,2-TRICHLOROETHOXYCARBONYLAMINO)-ALPHA-D-GLUCOPYRANOSIDE
acetic acid, [[1-[(2-chlorophenyl)methyl]-1H-benzimidazol-2-yl]thio]-, 2-[(E)-(4-chloro-3-nitrophenyl)methylidene]hydrazide
(2S,5R,1'S)-2-(tert-butyl)-5-[1'-hydroxy1'-(4-bromophenyl)methyl]-5-phenyl-1,3-dioxolane-4-one
(2S,5R,1'R)-2-(tert-butyl)-5-[1'-hydroxy1'-(4-bromophenyl)methyl]-5-phenyl-1,3-dioxolane-4-one
8,15-DI-O-TRICHLOROACETYLCARBAMOYL-11BETA,13-DIHYDROUROSPERMAL A FROMUROSPERMUM DELECHAMPII
Title Journal or Book Year
First Asymmetric Hetero Diels−Alder Reaction of 1-Sulfinyl Dienes with Nitroso Derivatives. A New Entry to the Synthesis of Optically Pure 1,4-Imino-l-ribitol Derivatives Organic Letters 2000
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