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(1'R,2R,5R,6R)-2-TERT.-BUTYL-6-METHYL-5-(1'-METHYLPENTYL)-1,3-DIOXAN-4-ONE

Compound with spectra: 2 NMR

(1'R,2R,5R,6R)-2-TERT.-BUTYL-6-METHYL-5-(1'-METHYLPENTYL)-1,3-DIOXAN-4-ONE
SpectraBase Compound ID IM7npcOF5W5
InChI InChI=1S/C15H28O3/c1-7-8-9-10(2)12-11(3)17-14(15(4,5)6)18-13(12)16/h10-12,14H,7-9H2,1-6H3/t10-,11-,12?,14-/m1/s1
InChIKey PTDZLWYNNDSXRD-XHMIPKSJSA-N
Mol Weight 256.39 g/mol
Molecular Formula C15H28O3
Exact Mass 256.203845 g/mol
Enantiomer InChIKey PTDZLWYNNDSXRD-XYXXDAQMSA-N

View Spectrum of (1'R,2R,5R,6R)-2-TERT.-BUTYL-6-METHYL-5-(1'-METHYLPENTYL)-1,3-DIOXAN-4-ONE

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

View Spectrum of (1'R,2R,5R,6R)-2-TERT.-BUTYL-6-METHYL-5-(1'-METHYLPENTYL)-1,3-DIOXAN-4-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1'S,2R,5R,6R)-2-TERT.-BUTYL-6-METHYL-5-(1'-METHYLPENTYL)-1,3-DIOXAN-4-ONE
(1'S,2R,5S,6R)-2-(t-butyl)-5-(1'-hydroxyisobutyl)-6-methyl-1,3-dioxan-4-one
(1'S,2R,5R,6R)-2-TERT.-BUTYL-5-(1'-HYDROXY-ISOBUTYL)-6-METHYL-1,3-DIOXAN-4-ONE
(1'S,2R,5S,6R)-2-TERT.-BUTYL-5-(1'-HYDROXY-2'-BUTENYL)-6-METHYL-1,3-DIOXAN-4-ONE
(1'S,2R,5S,6R)-2-(t-butyl)-5-(1'-hydroxy-2'-butenyl)-6-methyl-1,3-dioxan-4-one
4H-1,3-Benzodioxin-4-one, 2-(1,1-dimethylethyl)hexahydro-, [2S-(2.alpha.,4a.beta.,8a.beta.)]-
(2R,4S,6R)-4-BUTYL-2-TERT.-BUTYL-6-METHYL-1,3-DIOXAN-5-CARBOXYLIC-ACID
(2R,6R)-2-t-butyl-5,5-diallyl-6-methyl-1,3-dioxan-4-one
(2R,5R,6R)-2-t-butyl-5-allyl-5,6-dimethyl-1,3-dioxan-4-one
2-t-Butyl-6-methyl-5-phenylseleno-[1,3]dioxan-4-one
1,3-Dioxan-4-one, 2-(1,1-dimethylethyl)-6-methyl-5-(phenylseleno)-, [2R-(2.alpha.,5.beta.,6.alpha.)]-
Title Journal or Book Year
(E,R,R)‐5‐Alkyliden‐2‐tert‐butyl‐6‐methyl‐1,3‐dioxan‐4‐one: Herstellung aus (R)‐3‐Hydroxybuttersäure, Cuprat‐Additionen und Hydrolysen zu 3‐Hydroxycarbonsäuren mit chiralen sekundären Alkylgruppen in 2‐Stellung Chemische Berichte 1990

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