TY - JOUR
T1 - Two diastereomeric artificial enzymes with different catalytic activity
AU - Lindbäck, Emil Anders
AU - Zhou, You
AU - Pedersen, Christian Marcus
AU - Bols, Mikael
PY - 2012/9
Y1 - 2012/9
N2 - Two epimeric cyclodextrin-6-C-aldehydes were synthesised in 10 steps from β-cyclodextrin. The synthesis involved protection/partial deprotection, oxidation to a 6-aldehyde, olefination, dihydroxylation, selective protection of the secondary alcohol and oxidation. The two isomers catalysed theoxidation of aromatic amines by hydrogen peroxide but predominantly outside the cavity. Hydrolysis of aryl glycosides on the other hand was catalysed in a reaction followingMichaelis-Menten kinetics. The S isomer was a 5-20 times better catalyst than the R isomer, which was explained from models.
AB - Two epimeric cyclodextrin-6-C-aldehydes were synthesised in 10 steps from β-cyclodextrin. The synthesis involved protection/partial deprotection, oxidation to a 6-aldehyde, olefination, dihydroxylation, selective protection of the secondary alcohol and oxidation. The two isomers catalysed theoxidation of aromatic amines by hydrogen peroxide but predominantly outside the cavity. Hydrolysis of aryl glycosides on the other hand was catalysed in a reaction followingMichaelis-Menten kinetics. The S isomer was a 5-20 times better catalyst than the R isomer, which was explained from models.
U2 - 10.1002/ejoc.201200699
DO - 10.1002/ejoc.201200699
M3 - Journal article
SN - 1434-193X
VL - 2012
SP - 5366
EP - 5372
JO - European Journal of Organic Chemistry
JF - European Journal of Organic Chemistry
IS - 27
ER -