Residue-specific peptide modification: a chemist's guide

JN deGruyter, LR Malins, PS Baran - Biochemistry, 2017 - ACS Publications
Advances in bioconjugation and native protein modification are appearing at a blistering
pace, making it increasingly time consuming for practitioners to identify the best chemical …

Electrophilic trifluoromethylation by use of hypervalent iodine reagents

J Charpentier, N Fruh, A Togni - Chemical reviews, 2015 - ACS Publications
1. INTRODUCTION This review article is concerned with the use of compounds 1 and 2
(Figure 1) as effective and very versatile reagents for trifluoromethylation reactions of a …

Synthetic Methods for Compounds Having CF3–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions

XH Xu, K Matsuzaki, N Shibata - Chemical reviews, 2015 - ACS Publications
1. INTRODUCTION Fluorine is the most abundant halogen in the Earth, s crust. 1 However,
only a dozen fluorinated organic compounds have been identified in nature. 2 Most of the …

Introduction of fluorine and fluorine‐containing functional groups

T Liang, CN Neumann, T Ritter - … Chemie International Edition, 2013 - Wiley Online Library
Over the past decade, the most significant, conceptual advances in the field of fluorination
were enabled most prominently by organo‐and transition‐metal catalysis. The most …

Recent advances in the trifluoromethylation methodology and new CF3-containing drugs

W Zhu, J Wang, S Wang, Z Gu, JL Aceña… - Journal of Fluorine …, 2014 - Elsevier
This review provides a brief assessment of the methodological field of trifluoromethylation
and its possible impact on the development of new CF 3-containing pharmaceuticals …

Einführung von Fluor und fluorhaltigen funktionellen Gruppen

T Liang, CN Neumann, T Ritter - Angewandte Chemie, 2013 - Wiley Online Library
Die wichtigsten konzeptionellen Fortschritt auf dem Gebiet der Fluorierungen der letzten
zehn Jahre wurden durch die Organo‐und Übergangsmetallkatalyse ermöglicht. Die …

Fundamental studies and development of nickel-catalyzed trifluoromethylthiolation of aryl chlorides: active catalytic species and key roles of ligand and traceless …

G Yin, I Kalvet, U Englert… - Journal of the American …, 2015 - ACS Publications
A catalytic protocol to convert aryl and heteroaryl chlorides to the corresponding
trifluoromethyl sulfides is reported herein. It relies on a relatively inexpensive Ni (cod) 2/dppf …

Trifluoromethyl ethers and–thioethers as tools for medicinal chemistry and drug discovery

G Landelle, A Panossian… - Current Topics in …, 2014 - ingentaconnect.com
The ever-growing number of fluorinated compounds in medicinal and agrochemical
applications has led to a remarkable positive emulation in research. The last few years have …

Benziodoxole-based hypervalent iodine reagents for atom-transfer reactions

JP Brand, DF González, S Nicolai… - Chemical …, 2011 - pubs.rsc.org
In the last decades, hypervalent iodine reagents have raised from chemical curiosities to
mainstream reagents in organic synthesis. The use of benziodoxole-derived reagents has …

Trifluoromethylthiolation of aryl iodides and bromides enabled by a bench‐stable and easy‐to‐recover dinuclear palladium (I) catalyst

G Yin, I Kalvet, F Schoenebeck - … Chemie International Edition, 2015 - Wiley Online Library
While palladium catalysis is ubiquitous in modern chemical research, the recovery of the
active transition‐metal complex under routine laboratory applications is frequently …