Publication:
Facile syntheses of 3-halo and mixed 3,5-dihalo analogues of N-acetye-L-tyrosine via sulfonic acid-catalysed regioselective monohalogenation.

Simple item page
dc.contributor.authorPakorn Bovonsombaten_US
dc.contributor.authorKhanthapura, P.en_US
dc.contributor.authorKrause, M.M.en_US
dc.contributor.authorLeykajarakul, J.en_US
dc.contributor.otherMahidol University International College, Science Division.en_US
dc.date.accessioned2015-06-18T04:27:13Z
dc.date.accessioned2018-03-08T08:23:37Z
dc.date.available2015-06-18T04:27:13Z
dc.date.available2018-03-08T08:23:37Z
dc.date.created2015
dc.date.issued2008
dc.description.abstractThe combination of catalytic amounts of p-toluenesulfonic acid and 1 equiv of N-halosuccinimide afforded highly selective ring-halogenation of N-acetyl-L-tyrosine, furnishing either N-acetyl-3-halo-L-tyrosine analogues or mixed 3,5-dihalo derivatives in a one-pot reaction with excellent yields at room temperature.en_US
dc.identifier.citationTetrahedron Letters. Vol. 49, No. 49 (2008), 7008-7011en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/9961
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.subjectp-toluenesulfonic acid,en_US
dc.subjectN-halosuccinimideen_US
dc.subjectN-acetyl-Ltyrosineen_US
dc.titleFacile syntheses of 3-halo and mixed 3,5-dihalo analogues of N-acetye-L-tyrosine via sulfonic acid-catalysed regioselective monohalogenation.en_US
dc.typeArticleen_US
dspace.entity.typePublication
mods.location.urlhttps://www.sciencedirect.com/science/article/pii/S0040403908017978

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description:
Download

Collections

MUIC-Article