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(2-S,1'-R,4'-R)-(4'-METHYLCYCLOPENT-2'-ENYL)-GLYCINE;L-CARBAFURANOMYCIN

Compound with spectra: 1 NMR

(2-S,1'-R,4'-R)-(4'-METHYLCYCLOPENT-2'-ENYL)-GLYCINE;L-CARBAFURANOMYCIN
SpectraBase Compound ID 1apNkHGl9lU
InChI InChI=1S/C8H13NO2/c1-5-2-3-6(4-5)7(9)8(10)11/h2-3,5-7H,4,9H2,1H3,(H,10,11)/t5-,6-,7-/m0/s1
InChIKey MLYJMHSOUKWHHS-ACZMJKKPSA-N
Mol Weight 155.2 g/mol
Molecular Formula C8H13NO2
Exact Mass 155.094629 g/mol
Enantiomer InChIKey MLYJMHSOUKWHHS-FSDSQADBSA-N

View Spectrum of (2-S,1'-R,4'-R)-(4'-METHYLCYCLOPENT-2'-ENYL)-GLYCINE;L-CARBAFURANOMYCIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
2-cyclopentene-1-malonic acid
(2R,3S)-4-PHENYLVALINE
(2R,3R)-4-PHENYLVALINE
(2S,3R)-4-PHENYLVALINE
(2S,3S)-4-PHENYLVALINE
(2R)-Cyclohexyl glycine ethyl ester
Cyclohexanecarboxylic acid, 2-ethenyl-, cis-
(E,2R,3R)-2-amino-3-hydroxy-octadec-4-enoic acid ethyl ester
anti-2-methyl-3-(2-methylprop-1-enyl)octanoic acid
(E)-2,6-diamino-2-methylhept-3-enedioic acid
Title Journal or Book Year
Synthesis of l-Carbafuranomycin, an Unnatural Analogue of the Antibiotic Amino Acid Furanomycin, Organic Letters 2005

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