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(1S,5S,6R,7R,8R)-1-O-ACETYL-5,6:7,8-BIS-(IOSPROPYLIDENEDIOXY)-3-CYCLOCTEN-1-OL

Compound with spectra: 1 NMR, and 1 MS (GC)

(1S,5S,6R,7R,8R)-1-O-ACETYL-5,6:7,8-BIS-(IOSPROPYLIDENEDIOXY)-3-CYCLOCTEN-1-OL
SpectraBase Compound ID 6E7FT5lPW2y
InChI InChI=1S/C16H24O6/c1-9(17)18-10-7-6-8-11-13(21-15(2,3)19-11)14-12(10)20-16(4,5)22-14/h6,8,10-14H,7H2,1-5H3/b8-6-/t10-,11+,12-,13-,14-/m1/s1
InChIKey HZPACJGPRKSFGZ-MSTQXEBZSA-N
Mol Weight 312.36 g/mol
Molecular Formula C16H24O6
Exact Mass 312.157288 g/mol
Enantiomer InChIKey HZPACJGPRKSFGZ-GHNRLXIRSA-N

View Spectrum of (1S,5S,6R,7R,8R)-1-O-ACETYL-5,6:7,8-BIS-(IOSPROPYLIDENEDIOXY)-3-CYCLOCTEN-1-OL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-67-3716-77

View Spectrum of (1S,5S,6R,7R,8R)-1-O-ACETYL-5,6:7,8-BIS-(IOSPROPYLIDENEDIOXY)-3-CYCLOCTEN-1-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1S,5S,6R,8R)-1-Acetyl-5,6:7,8-bis(isopropylidenedioxy)-3-cycloocten-1-ol
ETHYL-(Z)-(6,7,8-TRIDEOXY-1,2:3,4-DI-O-ISOPROPYLIDENE-alpha-D-GALACTONON-7-ENOPYRANOSID)-URONATE
2-HYDROXY-3-DEOXY-5,6:7,8-DI-O-ISOPROPYLIDENE-D-MANNO-2-OCTENO-1,4-LACTONE
(4S,5R,6S,7S)-4,5:6,7-BIS-(IOSPROPYLIDENEDIOXY)-2-CYCLOHEPTEN-1-ONE
2,3:4,5:6,7-TRI-O-ISOPROPYLIDENE-D-GLYCERO-D-GULO-HEPTOSE-TRIMETHYLENE-DITHIOACETAL
BJDABKDVPIJIGQ-QRTUWBSPSA-N
1,2:3,4-DI-O-ISOPROPYLIDENE-6-O-PIVALOYL-ALPHA-D-GALACTOPYRANOSE
Trimethylsilyl 1,2 : 3,4-di-O-isopropylidene-6,7-dideoxy-.alpha.-D-galacto-octapyranuronate
ETHYL-TRANS-2,3-DIDEOXY-4,5:7,8-DI-O-ISOPROPYLIDENE-6-O-TERT.-BUTYL-DIMETHYLSILYL-D-GLUCO-2-OCTONENATE
VJSTUPGYGJFVMG-WXDOIIRRSA-N
Bis-(1,2:3,4)-di-O-isopropylidene-.alpha.-D-galactopyranosyl) malonate
Title Journal or Book Year
Synthesis of Enantiomerically Pure, Highly Functionalized, Medium-Sized Carbocycles from Carbohydrates:  Formal Total Synthesis of (+)-Calystegine B2 The Journal of Organic Chemistry 2002

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