Optimizing the selectivity of DIFO-based reagents for intracellular bioorthogonal applications

Carbohydrate Research

Volumn 377, Issue , 2013, Pages 18-27

  Kim, Eun J ^a   Kang, Dong W ^b   Leucke, Hans F ^c   Bond, Michelle R ^c   Ghosh, Salil ^c   Love, Dona C ^c   Ahn, Jong Seog ^d   Kang, Dae Ook ^e   Hanover, John A ^c  

^a Daegu University   (South Korea)

^b Catholic University of Daegu   (South Korea)

^c NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^d Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

^e Changwon National University   (South Korea)

Author keywords

Copper catalyzed azide alkyne; Cycloaddition; Glycoconjugates; O GlcNAc; Strain promoted azide alkyne cycloaddition

Indexed keywords

CATALYSIS; CHEMICAL REACTIONS; COPPER; CYCLOADDITION; NITROGEN COMPOUNDS; REACTION RATES;

AZIDE-ALKYNE CYCLOADDITION; BIOORTHOGONAL REACTIONS; CARBON-CARBON TRIPLE BONDS; COPPER CATALYZED; ENHANCED REACTIVITY; FREE SULFHYDRYL GROUPS; GLYCOCONJUGATES; [3+2]-CYCLOADDITION;

HYDROCARBONS;

ALKYNE DERIVATIVE; AZIDE; FLUORINE DERIVATIVE; REAGENT; THIOL GROUP;

ARTICLE; ATOM; CHEMICAL REACTION; COVALENT BOND; CYCLOADDITION; CYTOSOL; ELECTRON; GLYCOSYLATION; PRIORITY JOURNAL;

EID: 84879048898     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2013.05.014     Document Type: Article

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