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(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#1

Compound with spectra: 2 NMR

(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#1
SpectraBase Compound ID B3fqGHpJSDJ
InChI InChI=1S/C12H22O2.CH2I.HI.Zn/c1-11(2)8-6-7-12(11,3)10(14-5)9(8)13-4;1-2;;/h8-10H,6-7H2,1-5H3;1H2;1H;/q;;;+1/p-1/t8-,9-,10-,12+;;;/m1.../s1
InChIKey PGOGVFIBUHROSR-LFXSUNLRSA-M
Mol Weight 531.52 g/mol
Molecular Formula C13H24I2O2Zn
Exact Mass 529.915712 g/mol
Parent InChIKey WWOMNZAVIQUEBC-VJVGBEBFSA-M
Enantiomer InChIKey PGOGVFIBUHROSR-JJLGXLETSA-M

View Spectrum of (R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#2
(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-ZINC-IODIDE
(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-(IODOMETHYL)-ZINC
Euchrenone b(16)
Suberitenone A
2-MERCAPTO-5,6,7,8,9,10,11,12-OCTAHYDRO-4-(2-THIENYL)CYCLODECA[b]PYRIDINE-3-CARBONITRILE
2-Benzyl-7-{2-[(4aR,5S,8aS)-1-methoxycarbonyl-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-5-yl]ethyl}-3-oxo-2,3-dihydro-1H-isoindole-4-carboxylic acid
ENT-(16R)-7-BETA,20-DIHYDROXY-KAURAN-15-ONE
Bis(trimethylsilyl) derivative of methyl ester of 3.alpha.,20.alpha.-Dihydroxy-5.beta.-pregnan-11-one-21-oic acid or Bis(trimethylsilyl) derivative of 17-Deoxy-.alpha.-cortolic acid
#34B;MINOR_ISOMER;(E)-3-(S),4-(S),5-(R)-TRIACETOXY-6-(S)-[(3,4,5-TRIMETHOXY)-(4'-METHOXY-3'-(PARA-TOLUENESULFONYLOXY)-2'-STILBENYLOXY)]-TETRAHYDROPYRAN-2(S)-C
19-ACETOXY-18-CHLORO-7,11-HAVANNADIOL
Title Journal or Book Year
Enantioselective Cyclopropanation of Allylic Alcohols. The Effect of Zinc Iodide The Journal of Organic Chemistry 1997
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