An Iron–Mesoionic Carbene Complex for Catalytic Intramolecular C–H Amination Utilizing Organic Azides

Author(s):  
Wowa Stroek ◽  
Martin Keilwerth ◽  
Daniel M. Pividori ◽  
Karsten Meyer ◽  
Martin Albrecht
2020 ◽  
Vol 913 ◽  
pp. 121195 ◽  
Author(s):  
Chang Cao ◽  
Guoliang Mao ◽  
Jun Cheng ◽  
Xuebing Leng ◽  
Liang Deng

2019 ◽  
Author(s):  
Maria Ines Leitao ◽  
Carmen Gonzalez ◽  
Zuzanna Filipiak ◽  
Ana Petronilho

<p>7-methylguanosine, the so-called mRNA cap 0 bears a very labile C8-H bond, due to the formation of an ylide/N-heterocyclic carbene, upon proton loss. The reaction of 7-methylguanosine with Pt(PPh3)4, via C-H oxidative addition, yields a hydrido–PtII carbene complex and this reactivity can be extrapolated to 7,9-dimethylguanine. </p>


2021 ◽  
Author(s):  
Josef Boronski ◽  
John Seed ◽  
Ashley Wooles ◽  
Stephen Liddle

Room temperature reaction of the uranium(IV)-carbene [U{C(SiMe3)(PPh2)}(BIPMTMS)(μ-Cl)Li(TMEDA)(μ-TMEDA)0.5]2 (1, BIPMTMS = C(PPh2NSiMe3)2) with white phosphorus (P4) produces the organo-P5 compound [P5{C(SiMe3)(PPh2)}2][Li(TMEDA)2] (2) and the uranium(IV)-methanediide [U{BIPMTMS}{Cl}{μ-Cl}2{Li(TMEDA)}] (3). This is an unprecedented...


2021 ◽  
Author(s):  
Nicholas Wiedmaier ◽  
Hartmut Schubert ◽  
Hermann A Mayer ◽  
Lars Wesemann

The ruthenium carbene pincer complex 2 was synthesized treating the benzo annulated cycloheptatriene bisphosphine 1 with RuCl3. Addition of three equivalents of hydrogen to the carbocyclic carbene complex 2 was...


Author(s):  
M. Cecilia Johnson ◽  
Dylan Rogers ◽  
Werner Kaminsky ◽  
Brandi M. Cossairt

Synthesis ◽  
2021 ◽  
Author(s):  
Zheng-Yang Gu ◽  
Yang Wu ◽  
Feng Jin ◽  
Bao Xiaoguang ◽  
Ji-Bao Xia

An atom- and step-economic intermolecular multi-component palladium-catalyzed C–H amidation of alkenes with carbon monoxide and organic azides has been developed for the synthesis of alkenyl amides. The reaction proceeds efficiently without an ortho-directing group on the alkene substrates. Nontoxic dinitrogen is generated as the sole by-product. Computational studies and control experiments have revealed that the reaction takes place via an unexpected mechanism by tandem palladium catalysis.


2014 ◽  
Vol 50 (80) ◽  
pp. 11961-11961 ◽  
Author(s):  
Daniela Intrieri ◽  
Paolo Zardi ◽  
Alessandro Caselli ◽  
Emma Gallo
Keyword(s):  

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