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(1S*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLPENTAN-1-OL

Compound with spectra: 1 NMR

(1S*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLPENTAN-1-OL
SpectraBase Compound ID 4F9AePyrKzU
InChI InChI=1S/C17H24O/c1-2-3-14-17(18,15-10-6-4-7-11-15)16-12-8-5-9-13-16/h4,6-8,10-12,16,18H,2-3,5,9,13-14H2,1H3/t16-,17?/m0/s1
InChIKey OIQJHUVOWXJFKG-BHWOMJMDSA-N
Mol Weight 244.38 g/mol
Molecular Formula C17H24O
Exact Mass 244.182715 g/mol
Enantiomer InChIKey OIQJHUVOWXJFKG-TZHYSIJRSA-N

View Spectrum of (1S*)-1-[(1R*)-CYCLOHEX-2-ENYL]-1-PHENYLPENTAN-1-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Procyclidine-A (-H2)
Trihexyphenidyl-M (HO-)
2-(4-Cyclopropyl-4-hydroxy-4-phenylbutyl)-2-phenyl-1,3-dioxolane
TRANS-2-ISOPROPYLAMINO-1-PHENYL-CYCLOHEXANOL
(1S,2S,5R)-2-isopropyl-5-methyl-1-phenyl-cyclohexanol
2-isopropyl-5-methyl-1-phenyl-cyclohexanol
1-(1-Cyclopentenyl)-1-phenylheptan-1-ol
(1R,2R,4R)-4-tert-butyl-1-phenyl-cyclohexane-1,2-diol
EXO-2-(4'-CHLORO-PHENYL)-BICYCLO-[2.2.1]-HEPTAN-ENDO-2-OL
ENDO,ENDO-7-BROMO-6-PHENYLBICYCLO[3.1.1]HEPTAN-6-OL
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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