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[3S,6R,(S)-R]-N-BENZYLOXYCARBONYL-3,6-DIHYDRO-3-METHYL-6-(PARA-TOLYLSULFINYL)-2H-1,2-OXAZINE

Compound with spectra: 1 NMR

[3S,6R,(S)-R]-N-BENZYLOXYCARBONYL-3,6-DIHYDRO-3-METHYL-6-(PARA-TOLYLSULFINYL)-2H-1,2-OXAZINE
SpectraBase Compound ID ER7cahiz2c4
InChI InChI=1S/C20H21NO4S/c1-15-8-11-18(12-9-15)26(23)19-13-10-16(2)21(25-19)20(22)24-14-17-6-4-3-5-7-17/h3-13,16,19H,14H2,1-2H3/t16-,19+,26?/m0/s1
InChIKey QBNYJDJMIZCXHD-PVULTXIPSA-N
Mol Weight 371.45 g/mol
Molecular Formula C20H21NO4S
Exact Mass 371.119129 g/mol
Enantiomer InChIKey QBNYJDJMIZCXHD-QGGXTUAISA-N

View Spectrum of [3S,6R,(S)-R]-N-BENZYLOXYCARBONYL-3,6-DIHYDRO-3-METHYL-6-(PARA-TOLYLSULFINYL)-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
N-(Benzyloxycarbonyl)-6-oxa-7-azabicyclo[3.2.2]non-8-en-3-one
N-(Benzyloxycarbonyl)-3.alpha.-hydroxy-6-oxa-7-azabicyclo[3.2.2]non-8-ene
Benzyl 5-tert-butyl-3-phenylisoxazole-2(3H)-carboxylate
(-)-(2-S,3-R,6-S,R(S))-6-METHYL-2-PHENYL-3-(PARA-TOLYLSULFINYL)-3,6-DIHYDRO-2H-PYRAN
[(1S,4S)-4-(Benzyloxycarbonyl-but-3-enyl-amino)-6-tert-butylsilanyloxy-cyclohept-2-enyl]-but-3-enyl-carbamic acid benzyl ester
N-Benzyloxycarbonyl-1-methyl-9-azabicyclo[4.2.1]nonan-7-ene
Benzenemethanol, .alpha.-[1-[(4-methylphenyl)sulfinyl]-2-propenyl]-2-nitro-, [.alpha.R*[S*(R*)]]-
(Rs)-5-Benzyloxy-5-hydroxymethyl-2-methoxy-2-(p-toluenesulfinylmethyl)tetrahydropyran
(3S*,4R*,sS*)-tert-Butyl 4-chloro-3-(2-furyl)-4-(p-tolylsulfinyl)butanoate
N-BENZYLOXYCARBONYL-3-BUTANOYLTETRAMIC-ACID
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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