Results 11 to 20 of about 300 (133)

A General Group Testing Strategy for Discovering Chemical Cooperativity. [PDF]

open access: yesAngew Chem Int Ed Engl
A combinatorial design theory‐based group testing strategy coupled with luminescence screening to uncover cooperative interactions in a large combinatorial space. Iterative deconvolution identifies reactive molecular pairs and enables the discovery of trifluoromethylthiolation (SCF3) reagents.
Pflüger PM   +9 more
europepmc   +3 more sources

Bis(trifluoromethyl)disulfide and the EtP<sub>4</sub> Phosphazene Base-Formation of a Bench-Stable [EtP<sub>4</sub>SCF<sub>3</sub>]<sup>+</sup>[SCF<sub>3</sub>]<sup>-</sup> Salt. [PDF]

open access: yesChemistry
The synthesis of a bench‐stable trifluoromethylthiolate‐substituted phosphazenium salt is reported. Reaction of bis(trifluoromethyl)disulfide with the EtP4 phosphazene base furnishes this salt in quantitative yield. The compound features a unique trifluoromethylthiolate‐iminium motif and allows for functionalization of both trifluoromethylthiolate ...
Hartmann L   +6 more
europepmc   +2 more sources

Metal Free Synthesis of Seven-Membered Biaryl Sultams. [PDF]

open access: yesChem Asian J
A simple, metal‐free denitrogenative cyclization of benzothiatriazines enables efficient access to seven‐membered biaryl sultams under thermal conditions. The reaction tolerates diverse functional groups, and mechanistic studies, including radical trapping and EPR analysis, support a diradical pathway, providing new insights into sultam formation ...
Aman H   +8 more
europepmc   +2 more sources

Synthesis and Use of Trifluoromethylthiolated Ketenimines [PDF]

open access: yesChemistry – A European Journal, 2020
AbstractThe synthesis of trifluoromethylthiolated ketenimines is herein described. They are easily synthesized from the corresponding α‐trifluoromethylthiolated oximes upon activation with triflic anhydride and a base. The presumed nitrilium ion resulting from the Beckmann rearrangement is deprotonated to lead to the key intermediate, whose stability ...
Leroux, Frédéric R.   +6 more
openaire   +3 more sources

Recent Advances in Bioconjugation of Aromatic Amino Acid Residues by a Reactivity-Guided Approach. [PDF]

open access: yesChem Rec
This review highlights recent advances in the bioconjugation of aromatic amino acids residues, focusing on strategies that leverage their inherent chemical reactivity to enable precise and versatile modifications of biomacromolecules, illustrating relevant applications.
Santos BMDS   +3 more
europepmc   +2 more sources

Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review

open access: yesMolecules, 2020
In this review, recent advances over the past decade in the preparation of fluorinated stereogenic quaternary centers on β-keto esters compounds are analyzed.
Albert Granados, Adelina Vallribera
doaj   +1 more source

Recent Advances of Direct Trifluoromethylthiolation [PDF]

open access: yesChinese Journal of Organic Chemistry, 2015
Ke Zhang, Xiuhua Xu, Fengling Qing
exaly   +2 more sources

Difluorocarbene‐Derived Trifluoromethylthiolation and [18F]Trifluoromethylthiolation of Aliphatic Electrophiles [PDF]

open access: yesAngewandte Chemie International Edition, 2015
AbstractThe first trifluoromethylthiolation and [18F]trifluoromethylthiolation of alkyl electrophiles with in situ generated difluorocarbene in the presence of elemental sulfur and external (radioactive) fluoride ion is described. This transition‐metal‐free approach is high yielding, compatible with a variety of functional groups, and operated under ...
Jian, Zheng   +4 more
openaire   +2 more sources

Recent Synthetic Advances in C-H/N-H Functionalization of 1H-Pyrazoles: Diverse Strategies Across Variously Substituted Scaffolds. [PDF]

open access: yesChem Rec
Systematic overview of pyrazole functionalization reactions from C‐5 to N−H. It covers different strategies, from traditional cross‐coupling of prefunctionalized pyrazoles to more efficient direct functionalizations. This review briefly and systematically overviews C–H and N–H functionalization reactions of pyrazoles, aimed at creating new CC and C ...
Dzedulionytė Müldür K   +3 more
europepmc   +2 more sources

Direct electrophilic N-trifluoromethylthiolation of amines with trifluoromethanesulfenamide

open access: yesBeilstein Journal of Organic Chemistry, 2013
The CF3SN moiety is a substituent with interesting properties. However, there is no easy synthetic access to molecules bearing this group. The trifluoromethanesulfenamide is a new reagent for the electrophilic trifluoromethylthiolation which reacts ...
Sébastien Alazet   +2 more
doaj   +1 more source

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