Metal-catalyzed Markovnikov-type selective hydrofunctionalization of terminal alkynes

J Chen, WT Wei, Z Li, Z Lu - Chemical Society Reviews, 2024 - pubs.rsc.org
Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes
provides a straightforward and atom-economical route to access 1, 1-disubstituted alkenes …

Gold (I)-catalyzed activation of alkynes for the construction of molecular complexity

R Dorel, AM Echavarren - Chemical reviews, 2015 - ACS Publications
For centuries, gold had been considered a precious, purely decorative inert metal. It was not
until 1986 that Ito and Hayashi described the first application of gold (I) in homogeneous …

Late transition metal-catalyzed hydroamination and hydroamidation

L Huang, M Arndt, K Gooßen, H Heydt… - Chemical …, 2015 - ACS Publications
This Review examines recent developments in late transition metal-catalyzed
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …

Gold-catalyzed carbon− heteroatom bond-forming reactions

A Corma, A Leyva-Pérez, MJ Sabater - Chemical reviews, 2011 - ACS Publications
After the long-held assumption of the unreactivity of gold, numerous reactions catalyzed by
this noble metal have been increasingly emerging in the literature over the past 2 decades …

The development and catalytic uses of N-heterocyclic carbene gold complexes

SP Nolan - Accounts of chemical research, 2011 - ACS Publications
Gold has emerged as a powerful synthetic tool in the chemist's arsenal. From the early use
of inorganic salts such as AuCl and AuCl3 as catalysts, the field has evolved to explore …

Design and evolution of chimeric streptavidin for protein-enabled dual gold catalysis

F Christoffel, NV Igareta, MM Pellizzoni… - Nature Catalysis, 2021 - nature.com
Artificial metalloenzymes result from anchoring an organometallic catalyst within an
evolvable protein scaffold. Thanks to its dimer of dimers quaternary structure, streptavidin …

Transition metal-catalyzed addition of C-, N-and O-nucleophiles to unactivated C–C multiple bonds

NT Patil, RD Kavthe, VS Shinde - Tetrahedron, 2012 - Elsevier
The additions of various nucleophiles (XeH) to carbonecarbon (CeC) multiple bonds are of
prime importance in synthetic organic chemistry. These essentially simple reactions allow …

Redox‐switchable ring‐closing metathesis: Catalyst design, synthesis, and study

K Arumugam, CD Varnado Jr… - … A European Journal, 2013 - Wiley Online Library
High yielding syntheses of 1‐(ferrocenylmethyl)‐3‐mesitylimidazolium iodide (1) and 1‐
(ferrocenylmethyl)‐3‐mesitylimidazol‐2‐ylidene (2) were developed. Complexation of 2 to …

Homogeneous Gold‐Catalyzed Cyclization Reactions of Alkynes with N‐ and S‐Nucleophiles

W Debrouwer, TSA Heugebaert… - Advanced Synthesis …, 2015 - Wiley Online Library
This review covers the formation of N‐and S‐containing heterocycles, initiated by gold‐
catalyzed nucleophilic attack of N‐or S‐nucleophiles onto alkynes. These types of …

Direct synthesis of quinazolines through copper-catalyzed reaction of aniline-derived benzamidines

Y Ohta, Y Tokimizu, S Oishi, N Fujii, H Ohno - Organic Letters, 2010 - ACS Publications
A novel synthesis of 2-phenyl-4-[(triisopropylsilyl) methyl] quinazolines from
monosubstituted arenes has been developed. Treatment of N-phenylbenzamidines with 5 …