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#35;(2R*,3S*,5R*)-(+/-)-5-[[BIS-(1,1-DIMETHYLETHYL)-ETHYLSILYL]-OXY]-2-[(4-FLOUROPHENOXY)-THIOCARBONYLOXY]-3-(METHOXYMETHOXY)-6-OCTYN-1-YL-2,2-DIMETHYLPROPIONA

Compound with spectra: 1 NMR

#35;(2R*,3S*,5R*)-(+/-)-5-[[BIS-(1,1-DIMETHYLETHYL)-ETHYLSILYL]-OXY]-2-[(4-FLOUROPHENOXY)-THIOCARBONYLOXY]-3-(METHOXYMETHOXY)-6-OCTYN-1-YL-2,2-DIMETHYLPROPIONA
SpectraBase Compound ID DYful4zL9pn
InChI InChI=1S/C37H53FO8SSi/c1-35(2,3)33(39)42-25-32(45-34(47)44-29-20-18-28(38)19-21-29)31(43-26-40-10)23-30(46-48(36(4,5)6)37(7,8)9)17-14-22-41-24-27-15-12-11-13-16-27/h11-13,15-16,18-21,30-32,48H,22-26H2,1-10H3/t30-,31+,32+/m1/s1
InChIKey DZBRIQIGOJIXSY-RTOKGZNSSA-N
Mol Weight 705.0 g/mol
Molecular Formula C37H53FO8SSi
Exact Mass 704.321445 g/mol
Enantiomer InChIKey DZBRIQIGOJIXSY-DCMFLLSESA-N

View Spectrum of #35;(2R*,3S*,5R*)-(+/-)-5-[[BIS-(1,1-DIMETHYLETHYL)-ETHYLSILYL]-OXY]-2-[(4-FLOUROPHENOXY)-THIOCARBONYLOXY]-3-(METHOXYMETHOXY)-6-OCTYN-1-YL-2,2-DIMETHYLPROPIONA

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
5,6,7-Tri-O-benzyl-2,2,3,3-tetradehydro-2,3-dideoxy-8-O-pivaloyl-D-ido-octose diethyl acetal
(4R,5R)-4-[tert-butyl(diphenyl)silyl]oxy-5-(2-phenylmethoxyethyl)-2-oxolanone
METHYL-2-O-ACETYL-3-O-BENZYL-5-O-TERT.-BUTYLDIMETHYLSILYL-ALPHA-D-ARABINOFURANOSIDE
Benzyl 4-O-benzyl-2,6-di-O-methyl.alpha.-D-glucopyranoside
LANCEOLOSIDE-A
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 4-hydroxybenzoate
Methyl 3-deoxy-.beta.,D-ribo-hexopyranoside Tri-O-benzoate
6'-O-GALLOYLSALIDROSIDE
2,5,6-Tri-O-benzoyl-3-deoxygulono-.gama.-lactone
tert-butyl-[(1R)-1-[(4S,5R)-2,2-dimethyl-5-(phenylmethoxymethyl)-1,3-dioxolan-4-yl]but-3-ynoxy]-dimethyl-silane
Title Journal or Book Year
Applications of 5-Endo-trigonal Cyclization:  Construction of Compounds Relevant to the Synthesis of Prostaglandins and Methyl epi-Jasmonate The Journal of Organic Chemistry 1999
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