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(2S,3aS,4S,5S)-2-(2-Bromophenyl)-4,5-bis-(tert-butyldimethylsilyloxy)hexahydropyrrolo[1,2-b][1,2]oxazole

Compound with spectra: 1 NMR, and 1 MS (GC)

(2S,3aS,4S,5S)-2-(2-Bromophenyl)-4,5-bis-(tert-butyldimethylsilyloxy)hexahydropyrrolo[1,2-b][1,2]oxazole
SpectraBase Compound ID D3QPiFiK4cE
InChI InChI=1S/C24H42BrNO3Si2/c1-23(2,3)30(7,8)28-21-16-26-19(22(21)29-31(9,10)24(4,5)6)15-20(27-26)17-13-11-12-14-18(17)25/h11-14,19-22H,15-16H2,1-10H3/t19-,20-,21-,22-/m0/s1
InChIKey YQSUAIZLMYKTRL-CMOCDZPBSA-N
Mol Weight 528.7 g/mol
Molecular Formula C24H42BrNO3Si2
Exact Mass 527.18866 g/mol
Enantiomer InChIKey YQSUAIZLMYKTRL-GXRSIYKFSA-N

View Spectrum of (2S,3aS,4S,5S)-2-(2-Bromophenyl)-4,5-bis-(tert-butyldimethylsilyloxy)hexahydropyrrolo[1,2-b][1,2]oxazole

MS (GC) Spectrum
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Source of Spectrum U1-2013-4883-10a

View Spectrum of (2S,3aS,4S,5S)-2-(2-Bromophenyl)-4,5-bis-(tert-butyldimethylsilyloxy)hexahydropyrrolo[1,2-b][1,2]oxazole

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(5R,7S,8S)-7,8-Bis(tert-butyldimethylsiloxy)-2-phenylbicyclo[3.3.0]oct-1-en-3-one
TERREUMOL_C
2,3-Dihydroxy-1,8-di-methyl-7H-thiazolo[3,2-b]-benzo[1,2,4]triazin-7-one
[(2R,3S,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3-butanoyloxy-tetrahydrofuran-2-yl]methyl butanoate
Dimethyl 2-benzoyl-2-ethyl-3-(4-nitrophenyl)-1,1-cyclopropanedicarboxylate
TERT.-BUTYL-(3AR,4S,5S,7S)-4-ACETAMIDO-5-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-3,3A,4,5,6,7-HEXAHYDROPYRIDO-[1,2-C]-[1,2,3]-TRIAZOLE-7-CARBOXYLATE
[(8R,9S,10S,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
5β-Pregnane-3α,20β-diol, 3-acetate
8b-Isopropenyl-7-methoxy-2a-methyl-1,2a,3,8b-tetrahydro-2H-cyclobuta[c]chromene
3H-Pyrrolo[3',4':3,4]pyrrolo[1,2-c]thiazole-6,8(1H,7H)-dione, tetrahydro-7-methyl-5-(2-phenylethenyl)-, (5.alpha.,5a.alpha.,8a.alpha.,8b.beta.)-
Title Journal or Book Year
Copper-Catalyzed Synthesis of a Highly Hydroxy-Functionalized Benzo[e]indolizidine by IntramolecularN-Arylation European Journal of Organic Chemistry 2013
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