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(2R,3AS,4S,5S)-2-(2-BROMOPHENYL)-4,5-DI-TERT.-BUTOXYHEXAHYDROPYRROLO-[1,2-B]-[1,2]-OXAZOLE

Compound with spectra: 1 NMR

(2R,3AS,4S,5S)-2-(2-BROMOPHENYL)-4,5-DI-TERT.-BUTOXYHEXAHYDROPYRROLO-[1,2-B]-[1,2]-OXAZOLE
SpectraBase Compound ID KC5I3ztz2zd
InChI InChI=1S/C20H30BrNO3/c1-19(2,3)23-17-12-22-15(18(17)24-20(4,5)6)11-16(25-22)13-9-7-8-10-14(13)21/h7-10,15-18H,11-12H2,1-6H3/t15-,16+,17-,18-/m0/s1
InChIKey HTRMQGZKDGOKOJ-MHORFTMASA-N
Mol Weight 412.37 g/mol
Molecular Formula C20H30BrNO3
Exact Mass 411.140907 g/mol
Enantiomer InChIKey HTRMQGZKDGOKOJ-XMTFNYHQSA-N

View Spectrum of (2R,3AS,4S,5S)-2-(2-BROMOPHENYL)-4,5-DI-TERT.-BUTOXYHEXAHYDROPYRROLO-[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
(2S,3aS,4S,5S)-2-(2-Bromophenyl)-4,5-di-tert-butoxyhexahydropyrrolo[1,2-b][1,2]oxazole
(2S,3AR,4S,5S)-2-(2-BROMOPHENYL)-4,5-DI-TERT.-BUTOXYHEXAHYDROPYRROLO-[1,2-B]-[1,2]-OXAZOLE
(2R,3aR,4S,5S)-2-(2-Bromophenyl)-4,5-di-tert-butoxyhexahydropyrrolo[1,2-b][1,2]oxazole
(2R,2'S,3AR,4R,5R,6R)-2-(2-ACETYLOXYPROPYL)-4,5-DIBENZYLOXY-6-(BENZYLOXYMETHYL)-HEXAHYDROPYRROLO-[1,2-B]-ISOXAZOLE
(2R,2'R,3AR,4R,5R,6R)-2-(2-ACETYLOXYPROPYL)-4,5-DIBENZYLOXY-6-(BENZYLOXYMETHYL)-HEXAHYDROPYRROLO-[1,2-B]-ISOXAZOLE
(3.alpha.,5.beta.)-3(R)-(2',2'-Dimethyl-1',3'-dioxolan-4'-yl)2-(phenylmethyl)-5-(phthalimidomethyl)-isoxazolidine
(2R,2'R,3AR,4R,5R,6R)-4,5-DIBENZYLOXY-6-(BENZYLOXYMETHYL)-2-(2-HYDROXYPROPYL)-HEXAHYDROPYRROLO-[1,2-B]-ISOXAZOLE
(2R,3AR,4R,5R,6R)-4,5-DIBENZYLOXY-6-(BENZYLOXYMETHYL)-2-(2-HYDROXYETHYL)-HEXAHYDROPYRROLO-[1,2-B]-ISOXAZOLE
3-{(Acetyloxy)[(1S)-1-phenyl-3-butenyl]amino}-1,2,3-trideoxy-4,5-O-(1-methylethylidene)-D-ribo-hex-1-enitol
(3S,4R,5S)-1-BENZOYL-5-BENZYLOXYMETHYL-3,4-DIBENZYLOXYPYRROLIDIN-2-ONE
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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