For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE

Compound with spectra: 1 NMR

(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
SpectraBase Compound ID 6FuqFcxbHer
InChI InChI=1S/C26H33NO5Si/c1-25(2,3)32-24(29)27-21-20(31-23(28)22(21)27)17-30-33(26(4,5)6,18-13-9-7-10-14-18)19-15-11-8-12-16-19/h7-16,20-22H,17H2,1-6H3/t20-,21-,22-,27?/m1/s1
InChIKey HDVDDMFUTAOZPM-LPOKKUQKSA-N
Mol Weight 467.6 g/mol
Molecular Formula C26H33NO5Si
Exact Mass 467.2128 g/mol
Enantiomer InChIKey HDVDDMFUTAOZPM-DLMFWBLPSA-N

View Spectrum of (1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
(3S,4R,5S)-3-ACETOXY-4-[(BENZYLOXYCARBONYL)-AMINO]-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-TETRAHYDROFURAN-2-ONE
N(DELTA)-(5-TERT.-BUTYLDIPHENYLSILYL-ALPHA-D-RIBOFURANOSYL)-N(ALPHA)-BENZYLOXYCARBONYL-GLUTAMINE-BENZYLESTER
3-O-BENZYL-5-O-TERT.-BUTYL-DIPHENYLSILYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSE
(2R,3R,4S,5S,6S)-6-tert-Butyldiphenylsilyloxymethyl-3,5-diacetoxy-2-methoxy-4-methyl-3,4,5,6-tetrahydro-2H-pyran
2,3,4-TRI-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-ALPHA-D-MANNOPYRANOSIDE
(+/-)-(4R*,5R*,6S*)-5-(BENZYLOXY)-4-(TERT.-BUTYLDIPHENYLSILYLOXYMETHYL)-2,2-DIMETHYL-6-PHENYL-1,3-DIOXANE
2'-MERCAPTOETHYL-4-AZIDO-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-1,2,4-TRIDEOXY-1-THIO-ALPHA-D-ARABINO-HEXOSIDE
2'-MERCAPTOETHYL-4-AZIDO-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-1,2,4-TRIDEOXY-1-THIO-BETA-D-ARABINOSE-HEXOSIDE
METHYL-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-2-DEOXY-4-O-METHYLSULFONYL-ALPHA-D-XYLO-HEXOSIDE
Title Journal or Book Year
Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology European Journal of Organic Chemistry 2009
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.