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[(4aR,6R,7S,8S,8aR)-7-iodo-2,2-dimethyl-6-(2-trimethylsilylethylsulfonylamino)-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-8-yl] acetate

Compound with spectra: 1 NMR

[(4aR,6R,7S,8S,8aR)-7-iodo-2,2-dimethyl-6-(2-trimethylsilylethylsulfonylamino)-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-8-yl] acetate
SpectraBase Compound ID BColj648eXU
InChI InChI=1S/C16H30INO7SSi/c1-10(19)23-14-12(17)15(18-26(20,21)7-8-27(4,5)6)24-11-9-22-16(2,3)25-13(11)14/h11-15,18H,7-9H2,1-6H3/t11-,12+,13-,14-,15-/m1/s1
InChIKey FTIXXGOOZYNFSY-XLWJZTARSA-N
Mol Weight 535.47 g/mol
Molecular Formula C16H30INO7SSi
Exact Mass 535.055695 g/mol
Enantiomer InChIKey FTIXXGOOZYNFSY-AICCOOGYSA-N

View Spectrum of [(4aR,6R,7S,8S,8aR)-7-iodo-2,2-dimethyl-6-(2-trimethylsilylethylsulfonylamino)-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-8-yl] acetate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
NVAJDAQRNVWUBR-JJTUDDRGSA-N
NVAJDAQRNVWUBR-ZHCJQAHYSA-N
(4aR,5aS,9R,10aS,11R,11aR)11-(p-Bromobenzoyloxy)-4,4a,5a,6,9,10a,11,11a-decahydrooxepino[2',3':5,6]pyrano[3,2-d]-1.3-dioxin-9-methanol
2-TRIFLUOROACETAMIDOETHYL 3-O-ACETYL-2-O-BENZOYL-4,6-O-ISOPROPYLIDENE-ALPHA-D-MANNOPYRANOSIDE
2,6-Anhydro-9-O-(tert-butyldimethylsilyl)-7,8-dideoxy-1,3-O-isopropylidene-4-O-(2,2-dimethylpropionyl)-D-gluco-L-glycero-nonit-7-yl allyl ether
1,3-Dioxolo[4,5]pyrano[3,2-d][1,3]dioxin, acetamide deriv.
6-ISOTHIOCYANATO-N-[BIS-[3-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL)-THIOUREIDOMETHYL]-METHYL]-HEXANAMIDE
2-TRIFLUOROACETAMIDOETHYL 2,3-DI-O-BENZOYL-4,6-O-ISOPROPYLIDENE-ALPHA-D-MANNOPYRANOSIDE
1-DEOXY-1-[3-(4-PHENOXYPHENYL)-2-THIOUREIDO]-B-D-GLUCOPYRANOSE 2,3,4,6-
(-)-Bis(1,2:5,6-Di-O-Isopropylidene-.alpha.,D-glucofuranosyl)naphthalene-2,6-dicarboxylate
Title Journal or Book Year
Facile C1 Epimerization of α-1-Sulfonamidyl-2-deoxy-2-iodo- glycopyranosides The Journal of Organic Chemistry 2001
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