A novel simplified synthesis of acivicin

A novel simplified synthesis of acivicin

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http://www.wikidata.org/entity/Q58853261
Three-dimensional heterocycles: new uracil-based structures obtained by nucleophilic substitution at the sp2 carbon of bromoisoxazoline.Synthesis and in vitro/in vivo evaluation of the antitrypanosomal activity of 3-bromoacivicin, a potent CTP synthetase inhibitor.Synthesis and biological evaluation of papain-family cathepsin L-like cysteine protease inhibitors containing a 1,4-benzodiazepine scaffold as antiprotozoal agents.Synthesis and biological evaluation of CTP synthetase inhibitors as potential agents for the treatment of African trypanosomiasis.A continuous flow process using a sequence of microreactors with in-line IR analysis for the preparation of N,N-diethyl-4-(3-fluorophenylpiperidin-4-ylidenemethyl)benzamide as a potent and highly selective δ-opioid receptor agonist.Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.Inspired by Nature: The 3-Halo-4,5-dihydroisoxazole Moiety as a Novel Molecular Warhead for the Design of Covalent Inhibitors.Synthesis of l -Tricholomic Acid Analogues and Pharmacological Characterization at Ionotropic Glutamate Receptors
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A novel simplified synthesis of acivicin

Item
http://www.wikidata.org/entity/Q58853261
description
im März 2009 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в березні 2009
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name
A novel simplified synthesis of acivicin
@en
A novel simplified synthesis of acivicin
@nl
type
label
A novel simplified synthesis of acivicin
@en
A novel simplified synthesis of acivicin
@nl
prefLabel
A novel simplified synthesis of acivicin
@en
A novel simplified synthesis of acivicin
@nl
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A novel simplified synthesis of acivicin
@en
P304
P31
P356
10.1016/J.TETASY.2009.02.010
P433
P478
P50
P577