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#6;(3R,4S,5R,4'R,5'S)-2-BENZYL-3-[5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,4,5,6-TETRAHYDRO-2H-[1,2]-OXAZINAN-5-OL

Compound with spectra: 1 NMR

#6;(3R,4S,5R,4'R,5'S)-2-BENZYL-3-[5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,4,5,6-TETRAHYDRO-2H-[1,2]-OXAZINAN-5-OL
SpectraBase Compound ID LDiCkbUClQy
InChI InChI=1S/C24H41NO6Si/c1-23(2,3)32(7,8)29-16-19-22(31-24(4,5)30-19)20-21(27-6)18(26)15-28-25(20)14-17-12-10-9-11-13-17/h9-13,18-22,26H,14-16H2,1-8H3/t18-,19-,20-,21+,22+/m0/s1
InChIKey SENKFOHDHRDGOS-RTOMLYRKSA-N
Mol Weight 467.7 g/mol
Molecular Formula C24H41NO6Si
Exact Mass 467.270315 g/mol
Enantiomer InChIKey SENKFOHDHRDGOS-YXIAPDDASA-N

View Spectrum of #6;(3R,4S,5R,4'R,5'S)-2-BENZYL-3-[5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,4,5,6-TETRAHYDRO-2H-[1,2]-OXAZINAN-5-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
ANTI-(3S,4'R,5'S)-2-BENZYL-3-[5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,6-DIHYDRO-2H-[1,2]-OXAZINE
SYN-(3R,4'R,5'S)-2-BENZYL-3-[5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,6-DIHYDRO-2H-[1,2]-OXAZINE
[1,3]Dioxolo[4,5-d]isoxazol-5-one, tetrahydro-2-(phenylmethyl)-3-(2,2,5-trimethyl-1,3-dioxolan-4-yl)-, [3.alpha.-(4R*,5R*),3a.alpha.,6a.alpha.]-(.+-.)-
(3S,2'R,4'S,5'R)-2-BENZYL-3-(5'-TERT.-BUTYLDIMETHYLSILOXY-2'-METHYL-1',3'-DIOXAN-4'-YL)-4-METHOXY-3,6-DIHYDRO-2H-1,2-OXAZINE
(3R,2'R,4'S,5'R)-2-BENZYL-3-(5'-TERT.-BUTYLDIMETHYLSILOXY-2'-METHYL-1',3'-DIOXAN-4'-YL)-4-METHOXY-3,6-DIHYDRO-2H-1,2-OXAZINE
(3S,4R,4aR,5R)-5-(Benzyloxy)-3,4-diacetoxy-2,3,4,4a,5,6,7,8-octahydropyrido[1,2-b][1,2]oxazin-8-one
1H-[1,3]Dioxolo[3,4]cyclopent[1,2-c]isoxazol-7-ol, hexahydro-1,5,5-trimethyl-, acetate(ester), [3aR-(3a.alpha.,3b.alpha.,6a.alpha.,7.alpha.,7a.alpha.)]-
(4S,5R,6R,7R,8R)-4-tert-Butyldimethylsilyloxy-5-acetamido-6,7:8,9-di-O-isopropylidene-1-nonynyl Bromide
Ethyl (3R,4R,6S,7S)-4-(Dibenzylamino)-3-hydroxy-6,7-(isopropylidenedioxy)-5-(methoxymethoxy)-8-[(p-toluenesulfonyl)oxy]octanoate
beta-D-glucopyranoside, 2-chlorophenyl 2-(acetylamino)-2-deoxy-4,6-O-(2-furanylmethylene)-
Title Journal or Book Year
Application of L-Erythrose-Derived Nitrones in the Synthesis of Polyhydroxylated Compounds via 3,6-Dihydro-2H-1,2-oxazine Derivatives European Journal of Organic Chemistry 2012
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