Advances of azide-alkyne cycloaddition-click chemistry over the recent decade

MS Singh, S Chowdhury, S Koley - Tetrahedron, 2016 - Elsevier
During the past years, a variety of scientific and methodological developments have been
achieved, which urge chemists to increase the tools of their arsenal to improve the ease and …

Discovery of bioactive molecules from CuAAC click-chemistry-based combinatorial libraries

X Wang, B Huang, X Liu, P Zhan - Drug Discovery Today, 2016 - Elsevier
Highlights•Advances in the combination of the CuAAC reaction with direct screening.•Before
library assembly, the bioisosteric potential of 1, 2, 3-triazole should be confirmed.•The …

Synthesis of many different types of organic small molecules using one automated process

J Li, SG Ballmer, EP Gillis, S Fujii, MJ Schmidt… - Science, 2015 - science.org
Small-molecule synthesis usually relies on procedures that are highly customized for each
target. A broadly applicable automated process could greatly increase the accessibility of …

Synthesis of a copper-supported triplet nitrene complex pertinent to copper-catalyzed amination

KM Carsch, IM DiMucci, DA Iovan, A Li, SL Zheng… - Science, 2019 - science.org
Terminal copper-nitrenoid complexes have inspired interest in their fundamental bonding
structures as well as their putative intermediacy in catalytic nitrene-transfer reactions. Here …

Design and synthesis of novel 1, 2, 3-triazole-dithiocarbamate hybrids as potential anticancer agents

YC Duan, YC Ma, E Zhang, XJ Shi, MM Wang… - European journal of …, 2013 - Elsevier
A series of novel 1, 2, 3-triazole-dithiocarbamate hybrids were designed, synthesized and
evaluated for anticancer activity against four selected human tumor cell lines (MGC-803 …

Transition-metal-free catalytic synthesis of 1, 5-diaryl-1, 2, 3-triazoles

SW Kwok, JR Fotsing, RJ Fraser, VO Rodionov… - Organic …, 2010 - ACS Publications
1, 5-Diarylsubstituted 1, 2, 3-triazoles are formed in high yield from aryl azides and terminal
alkynes in DMSO in the presence of catalytic tetraalkylammonium hydroxide. The reaction is …

Triazole–dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration

YC Zheng, YC Duan, JL Ma, RM Xu, X Zi… - Journal of medicinal …, 2013 - ACS Publications
Lysine specific demethylase 1 (LSD1), the first identified histone demethylase, plays an
important role in epigenetic regulation of gene activation and repression. The up-regulated …

Design, synthesis, and structure–activity relationship of novel LSD1 inhibitors based on pyrimidine–thiourea hybrids as potent, orally active antitumor agents

LY Ma, YC Zheng, SQ Wang, B Wang… - Journal of medicinal …, 2015 - ACS Publications
Histone lysine specific demethylase 1 (LSD1) was reported to be overexpressed in several
human cancers and recognized as a promising anticancer drug target. In the current study …

“Clicking” polymer brushes with thiol-yne chemistry: indoors and out

RM Hensarling, VA Doughty, JW Chan… - Journal of the …, 2009 - ACS Publications
Thiol-yne click chemistry is demonstrated as a modular platform for rapid and practical
fabrication of highly functional, multicomponent surfaces under ambient conditions. The …

CalFluors: a universal motif for fluorogenic azide probes across the visible spectrum

P Shieh, VT Dien, BJ Beahm… - Journal of the …, 2015 - ACS Publications
Fluorescent bioorthogonal smart probes across the visible spectrum will enable sensitive
visualization of metabolically labeled molecules in biological systems. Here we present a …