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(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-BETA-D-ARABINOSE-HEXOSIDE
2'-MERCAPTOETHYL-4-AZIDO-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-1,2,4-TRIDEOXY-1-THIO-ALPHA-D-ARABINO-HEXOSIDE
METHYL-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-2-DEOXY-4-O-METHYLSULFONYL-BETA-D-LYXO-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
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