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(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-PENTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE

Compound with spectra: 1 NMR

(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-PENTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE
SpectraBase Compound ID LImdLaD19xG
InChI InChI=1S/C32H45N3O3Si/c1-7-8-11-16-25-22-35(34-33-25)28-21-24(29-30(28)38-32(5,6)37-29)23-36-39(31(2,3)4,26-17-12-9-13-18-26)27-19-14-10-15-20-27/h9-10,12-15,17-20,22,24,28-30H,7-8,11,16,21,23H2,1-6H3/t24-,28-,29-,30+/m1/s1
InChIKey BVWQUDCONBFEEY-MCILKKLMSA-N
Mol Weight 547.8 g/mol
Molecular Formula C32H45N3O3Si
Exact Mass 547.323019 g/mol
Enantiomer InChIKey BVWQUDCONBFEEY-DNEFNOKRSA-N

View Spectrum of (1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-PENTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-1-[4-(2-HYDROXYETHYL)-1H-1,2,3-TRIAZOL-1-YL]-2,3-ISOPROPYLIDENE-DIOXY-CYCLOPENTANE
(1R,2S,3R,4R)-1-[4-(ACETOXYMETHYL)-1H-1,2,3-TRIAZOL-1-YL]-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-CYCLOPENTANE
(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-PHENYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE
(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-METHOXYCARBONYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE
(1S,2S,3R,4R,6S)-4-(ACETOXYMETHYL)-6-(4-PENTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(1S,2S,3R,4R,6S)-4-(ACETOXYMETHYL)-6-(4-BUTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
TERT.-BUTYL-(E)-(3''-O-TERT.-BUTYLDIPHENYLSILYL-2',3'-O-ISOPROPYLIDENE-D-APIO-BETA-D-FURANOSYL)-3-CYANO-2-PROPENOATE
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-3'-DEOXY-3'-C-(HYDROXYMETHYL)-2'-O-(2-METHOXYETHYL)-5-METHYLURIDINE
(3S,4'R,5'S)-2-BENZYL-3-(5'-TERT.-BUTYLDIPHENYLSILYLOXYMETHYL-2',2'-DIMETHYL-1',3'-DIOXOLAN-4'-YL)-4-METHOXY-3,6-DIHYDRO-2H-[1,2]-OXAZINE
INTERMEDIATE-D
Title Journal or Book Year
Click Azide‐Alkyne Cycloaddition for the Synthesis of D‐(–)‐1,4‐Disubstituted Triazolo‐Carbanucleosides European Journal of Organic Chemistry 2009
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