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(+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXENOATE

Compound with spectra: 2 NMR

(+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXENOATE
SpectraBase Compound ID DuLS3KiaXIx
InChI InChI=1S/C29H34ClF2NO3/c1-20-12-17-24(28(2,3)21-9-6-5-7-10-21)25(19-20)36-26(34)11-8-18-29(31,32)27(30)33-22-13-15-23(35-4)16-14-22/h5-11,13-16,20,24-25H,12,17-19H2,1-4H3/b11-8+,33-27-/t20-,24-,25-/m1/s1
InChIKey UYYJWJBREHZOKP-LRSUVCFFSA-N
Mol Weight 518.0 g/mol
Molecular Formula C29H34ClF2NO3
Exact Mass 517.219528 g/mol
Enantiomer InChIKey UYYJWJBREHZOKP-YTSDDCPXSA-N

View Spectrum of (+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXENOATE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXANOATE
(+)-(2S,5S,1R)-5-METHYL-2-(1-METHYL-1-PHENYLETHYL)-CYCLOHEXYL-(Z)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-BUTENOATE
XQBRQPLBAKWFOB-MABODERHSA-N
XQBRQPLBAKWFOB-NJEFZAQSSA-N
(2S,5S,1R)-5-METHYL-2-(1-METHYL-1-PHENYLETHYL)-CYCLOHEXYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-BUTANOATE;MINOR-DIASTEREOMER
(2S,5S,1R)-5-METHYL-2-(1-METHYL-1-PHENYLETHYL)-CYCLOHEXYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-BUTANOATE;MAJOR-DIASTEREOMER
(1R,2S,5R)-8-Phenylmenthyl 2-Diazophenylacetate
(+/-)-8-Phenylmenthyl 2-oxocyclohexanecarboxylate
(-)-8-Phenylmenthyl 3-[2-(trimethylsilyl)ethenyl]cyclopropane-1-carboxylate
OAJJUFDHOYOSSA-JHVJFLLYSA-N
Title Journal or Book Year
Asymmetric Synthesis of Fluorinated Cyclic β-Amino Acid Derivatives through Cross Metathesis Organic Letters 2006
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