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(1R*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLETHANOL

Compound with spectra: 1 NMR

(1R*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLETHANOL
SpectraBase Compound ID 9BO7IQ75s9J
InChI InChI=1S/C14H18O/c1-14(15,12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2,4-6,8-10,13,15H,3,7,11H2,1H3/t13-,14+/m1/s1
InChIKey JFSDRQLNLFFPGO-KGLIPLIRSA-N
Mol Weight 202.3 g/mol
Molecular Formula C14H18O
Exact Mass 202.135765 g/mol
Enantiomer InChIKey JFSDRQLNLFFPGO-UONOGXRCSA-N

View Spectrum of (1R*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLETHANOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R*)-1-[(1S*)-CYCLOHEX-2-ENYL]-1-PHENYLETHANOL
2-((E)-1-Butenyl)-1-methoxy-1-phenylcyclopropane
3-(1-Hydroxy-1-phenylethyl)-1-phenylsulfenylpent-4-en-1-yne
4-Methyl-2-phenyl-3-trimethylsilylmethylpentan-2-ol
1-(1-Cyclohexen-1-yl)-1-phenylethanol
alpha-(1-BROMOHEPTYL)BENZHYDROL
alpha-(1-BROMOPENTYL)BENZHYDROL
alpha-(1-BROMODECYL)BENZHYDROL
alpha-(1-BROMOOCTYL)BENZHYDROL
alpha-(1-BROMONONYL)BENZHYDROL
Title Journal or Book Year
Diastereoselective Addition of γ-Substituted Allylic Nucleophiles to Ketones:  Highly Stereoselective Synthesis of Tertiary Homoallylic Alcohols Using an Allylic Tributylstannane/Stannous Chloride System Journal of the American Chemical Society 2002
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