In some cases, researchers have explored enzymatic methods, where enzymes are used to catalyze the formation of 4-amino-2(5H)-furanones. Enzymatic reactions can offer high selectivity and mild reaction conditions.
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(Z)-3-Amino-3-[1-(2-ethoxy-ethoxy)-cyclohexyl]-acrylic acid tert-butyl ester
5a-carba-α-D-mannopyranose-6-phosphate
(R)-2-nitro-1-(4-nitrophenyl)ethyl acetate
Phosphoric acid dibenzyl ester (2R,3R)-2,3-bis-benzyloxy-4-hydroxy-butyl ester
8-methoxycarbonyloctyl-4'-O-acetyl-2,3,6,2',6'-penta-O-benzoyl-β-D-lactoside
PORAPAK T (80-100 MESH ASTM) FOR GC
(S)-3-hydroxybutyryl-Coenzyme A
2,3-di-O-benzyl-D-ribose dibenzyl acetal
Glycine, N-[N-(N-acetyl-L-tyrosyl)glycyl]-, ethyl ester
benzyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->3)-2-acetamido-2-deoxy-α-D-galactopyranoside
5'-O-acetyl-2',3'-O-isopropylidene-6-(15)N-adenosine
S-Carboxymethyl-L-cysteine
m-(benzyloxycarbonyl)phenyl acetic acid
Decanal, oxime, (Z)-
