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[RH-(1,5-CYCLOOCTADIENE)-3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DIDEOXY-2,5-ANHYDRO-L-IDITOL]-BF4

Compound with spectra: 2 NMR

[RH-(1,5-CYCLOOCTADIENE)-3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DIDEOXY-2,5-ANHYDRO-L-IDITOL]-BF4
SpectraBase Compound ID Fp4TsqhmRIl
InChI InChI=1S/C30H30O3P2.C8H8.BF4.Rh/c1-23-29(32-34(25-15-7-3-8-16-25)26-17-9-4-10-18-26)30(24(2)31-23)33-35(27-19-11-5-12-20-27)28-21-13-6-14-22-28;1-2-4-6-8-7-5-3-1;2-1(3,4)5;/h3-24,29-30H,1-2H3;1-2,7-8H2;;/q;;2*-1/p+2/t23-,24-,29+,30+;;;/m1.../s1
InChIKey ZVTFKZUHZIKTTA-LPZZLRGXSA-P
Mol Weight 796.4 g/mol
Molecular Formula C38H40BF4O3P2Rh
Exact Mass 796.153677 g/mol
Parent InChIKey JZGYDNZMXFCEQR-YEHDKYDUSA-P
Enantiomer InChIKey ZVTFKZUHZIKTTA-KCCZOGKQSA-P

View Spectrum of [RH-(1,5-CYCLOOCTADIENE)-3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DIDEOXY-2,5-ANHYDRO-L-IDITOL]-BF4

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [RH-(1,5-CYCLOOCTADIENE)-3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DIDEOXY-2,5-ANHYDRO-L-IDITOL]-BF4

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[RH-(1,5-CYCLOOCTADIENE)-3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DIDEOXY-2,5-ANHYDRO-D-MANNITOL]-BF4
ARFBDXMJMHYUGK-UHFFFAOYSA-P
DESACETYLELEUTHEROBIN
BICYCLO-[2.2.1]-HEPTADIENE-1,4-BISDIPHENYLPHOSPHINOBUTANE-RHODIUM-(1)-TETRAFLUOROBORATE
17-(Cyclobutylmethyl)-3-methoxymorphinan-14-ol
3-Formyl-4-furyl-2-hydroxy-2-methyl-5-nitro-6-phenylcyclohexanecarboxylic acid methyl ester
Ethyl 3-bromo-7,8-difluoro-2-methyl-5-oxo-1,5-dihydropyrazolo[1,5-a]quinoline-4-carboxylate
KERMADECIN-F
cyclopentyl 4-(2-bromo-4,5-dimethoxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate
20,21-Dinoribogamin-18-ol, 2-ethyl-
N,7-bis(2-methoxyphenyl)-5-methyl-2-(methylsulfanyl)-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxamide
Title Journal or Book Year
C2-Symmetric Diphosphinite Ligands Derived from Carbohydrates. The Strong Influence of Remote Stereocenters on Asymmetric Rhodium-Catalyzed Hydrogenation The Journal of Organic Chemistry 2004
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