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[(1S,3R,4S,5R)-4-ACETYLAMINO-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANEDIMETHANOL-DIACETATE

Compound with spectra: 2 NMR

[(1S,3R,4S,5R)-4-ACETYLAMINO-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANEDIMETHANOL-DIACETATE
SpectraBase Compound ID 4HdCcA1F6Fg
InChI InChI=1S/C20H27NO5/c1-13(22)21-20(4)18(12-26-15(3)24)10-17(11-25-14(2)23)19(20)16-8-6-5-7-9-16/h5-9,17-19H,10-12H2,1-4H3,(H,21,22)/t17-,18+,19+,20-/m1/s1
InChIKey AYUIZVVYXSGNRT-FUMNGEBKSA-N
Mol Weight 361.44 g/mol
Molecular Formula C20H27NO5
Exact Mass 361.188923 g/mol
Enantiomer InChIKey AYUIZVVYXSGNRT-NMLBUPMWSA-N

View Spectrum of [(1S,3R,4S,5R)-4-ACETYLAMINO-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANEDIMETHANOL-DIACETATE

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

View Spectrum of [(1S,3R,4S,5R)-4-ACETYLAMINO-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANEDIMETHANOL-DIACETATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[(1R,3S,4R,5R)-4-ACETYLAMINO-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANEDIMETHANOL-DIACETATE
[(1S,3R,4S,5S)-4-(ACETYLAMINO)-4-METHYL-5-PHENYL]-1,3-CYCLOPENTANE-DIMETHANOL-DIACETATE
(1R*,2S*,8aR*)-Octahydro-8,8-dimethyl-1-phenyl-2-indolizinecarboxylic methyl ester
Racemic N-acetyl-r-2,c-4-di(acetoxymethyl)-2-methyl-c-5-(phenyl)pyrrolidine
(2S,3R,3aS,4R,6S,6aS)-2-amyl-4,6-dimethylol-3-phenyl-3,3a,4,5,6,6a-hexahydro-2H-pentalen-1-one
(+-)Methyl (1.alpha.,2a.beta.,8b.beta.)-2a-Hydroxy-1,2,2a,3,4,8b-hexahydrocyclobuta[a]naphthalene-1-carboxylate
(1R,2aS,8bR)-2a-hydroxy-2,3,4,8b-tetrahydro-1H-cyclobuta[a]naphthalene-1-carboxylic acid methyl ester
N-(tert-Butyl)-2-(4-chlorobenzoyl)-1-isopropyl-4-oxoazetidine-2-carboxamide
1-Benzyl-3-hydroxy-R-2,C-3-diphenyl-1-aza-6-oxa-cyclodecan-5-one
4,6-Bis(hydroxymethyl)-2-butyl-3-phenylhexahydropentalen-1(2H)-one
(2S,3R,3aS,4R,6S,6aS)-2-butyl-4,6-dimethylol-3-phenyl-3,3a,4,5,6,6a-hexahydro-2H-pentalen-1-one
Ethyl 2-acetylamino-2-cyano-3-(4-nitrophenyl)-5-oxo-5-(4-fluorophenyl)pentanoate
Title Journal or Book Year
Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process The Journal of Organic Chemistry 1998
Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. The Bridged Mode (β-Tether) The Journal of Organic Chemistry 1998
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