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(2S,3S,4R,5R)-2-(IODOMETHYL)-3,4,5-TRIHYDROXYTETRAHYDROTHIOPYRAN

Compound with spectra: 1 NMR

(2S,3S,4R,5R)-2-(IODOMETHYL)-3,4,5-TRIHYDROXYTETRAHYDROTHIOPYRAN
SpectraBase Compound ID 5k48v0Agils
InChI InChI=1S/C6H11IO3S/c7-1-4-6(10)5(9)3(8)2-11-4/h3-6,8-10H,1-2H2/t3-,4+,5+,6+/m0/s1
InChIKey GLIJKKDSHSONPY-SLPGGIOYSA-N
Mol Weight 290.12 g/mol
Molecular Formula C6H11IO3S
Exact Mass 289.94736 g/mol
Enantiomer InChIKey GLIJKKDSHSONPY-VANKVMQKSA-N

View Spectrum of (2S,3S,4R,5R)-2-(IODOMETHYL)-3,4,5-TRIHYDROXYTETRAHYDROTHIOPYRAN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent METHANOL-D4
(2R,3S,4R,5S)-2-(IODOMETHYL)-3,4,5-TRIHYDROXYTETRAHYDROTHIOPYRAN
D-GALACTITOL, 1-THIODECYL-
D-GALACTITOL, 1-THIODODECYL-
D-GALACTITOL, 1-THIOOCTYL-
D-GALACTOTOL, 1-THIONONYL-
D-Arabinose, dipropyl mercaptal
(1R,2S,3R)-1-(1,3-DITHIAN-2-YL)-BUTANE-1,2,3,4-TETROL
L-Mannose, 6-deoxy-, diethyl mercaptal
Disorbitylamine
(ERYTHRO)-3-DEOXY-D-MANNO-2-OCTULOSE
Title Journal or Book Year
Regio- and Stereospecific Me3SiI-Promoted Intramolecular Displacement of Hydroxy Group by Sulfide. 2. Polyhydroxylated Thiepane Ring Contraction to Thiolane or Thiane Derivatives. Synthesis of Enantiopure Polyalcohols1 The Journal of Organic Chemistry 1997

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