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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

Compound with spectra: 1 NMR

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
SpectraBase Compound ID G6BCHF2XETs
InChI InChI=1S/C24H39NO5Si/c1-23(2,3)31(7,8)28-17-20-22(30-24(4,5)29-20)21-19(26-6)14-15-27-25(21)16-18-12-10-9-11-13-18/h9-14,20-22H,15-17H2,1-8H3/t20-,21+,22+/m0/s1
InChIKey XRNBFXDKRVIBCS-BHDDXSALSA-N
Mol Weight 449.7 g/mol
Molecular Formula C24H39NO5Si
Exact Mass 449.25975 g/mol
Enantiomer InChIKey XRNBFXDKRVIBCS-FSSWDIPSSA-N

View Spectrum of 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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
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
(3S,4'R,5'S)-2-BENZYL-3-(5'-BENZYLOXYMETHYL-2',2'-DIMETHYL-1',3'-DIOXOLAN-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,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
[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.]-(.+-.)-
(3aS,5R,5aR,8aR,8bS)-5-Benzyloxy-1,7,7-trimethyl-octahydro-2,6,8-trioxa-1-aza-as-indacene
(4S,5R,6R,7R,8R)-4-tert-Butyldimethylsilyloxy-5-acetamido-6,7:8,9-di-O-isopropylidene-1-nonynyl Bromide
BENZYL-BENZYL-[(S)-1-[(4S,5R)-5-[(R)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-HYDROXYETHYL]-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-BUT-3-ENYL]-CARBAMATE
Dimethyl 2-[2',2'-dimethyl-tetrahydrofuro[3,4-d](1,3)-dioxol-4'-yl]isoxalidine-4,5-dicarboxylate
(4S,5R,6R,7R,8R)-4-tert-Butyldimethylsilyloxy-5-acetamido-6,7:8,9-di-O-isopropylidene-1-nonyne
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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