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NO NAME

Compound with spectra: 1 NMR

NO NAME
SpectraBase Compound ID 9L2cxN3osK8
InChI InChI=1S/C20H27NO4/c1-2-25-20(22)19-10-6-9-18(19)17(13-21)11-12-23-15-24-14-16-7-4-3-5-8-16/h3-5,7-8,17-19H,2,6,9-12,14-15H2,1H3/t17-,18+,19-/m0/s1
InChIKey HWOBJHMRBBTLSF-OTWHNJEPSA-N
Mol Weight 345.44 g/mol
Molecular Formula C20H27NO4
Exact Mass 345.194008 g/mol
Enantiomer InChIKey HWOBJHMRBBTLSF-CEXWTWQISA-N

View Spectrum of NO NAME

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R*,2R*,5R*)-2-Carbethoxy-6-oxobicyclo[3.3.0]octane
(1S,2R)-2-[(1S)-1-ethyl-2-keto-pentyl]cyclopentanecarboxylic acid methyl ester
2-NORBORNANEACETIC ACID, A-CYANO-, ETHYL ESTER
exo-Bicyclo[3.3.0]octane-2-carboxylic acid, 4-methylene-, methyl ester, cis-
Methyl 2-cyanobicyclo[3.2.1]octane-6-carboxylate
1H-Indene-1-carboxylic acid, octahydro-2-oxo-, methyl ester, (3a.alpha.,7a.beta.)-
2-Oxo-2,3,3aa, 4,5,6,7,7ab-octahydro-1H-indene-1-carboxylic acid, methyl ester
(4S,5S,8R,9S)-4-(HYDROXYMETHYL)-8-METHYLHEXAHYDROCYCLOPENTA-[C]-PYRANONE
(1R*,2R*,3S*)-3-Carbethoxy-2-(2-propenyl)cyclohexanecarboxylic acid
2-[(1R)-1-(2,2-diethoxyethyl)-2-methyl-allyl]-6-methyl-hept-6-enoic acid ethyl ester
Title Journal or Book Year
Formation of Functionalized Carbocycles via Base-Promoted Ring Opening/Brook Rearrangement/Allylic Alkylation of γ-Silyl-β,γ-epoxybutanenitrile Followed by Nitrile Anion Cyclization with Bis-Electrophiles Organic Letters 2004

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