Metal–organic frameworks: advanced tools for multicomponent reactions
The increasing demand for simple, clean, and sustainable protocols for the preparation of
complex organic molecules has continuously encouraged researchers to discover and …
complex organic molecules has continuously encouraged researchers to discover and …
Dinuclear gold (i) complexes: from bonding to applications
TACA Bayrakdar, T Scattolin, X Ma… - Chemical Society …, 2020 - pubs.rsc.org
The last two decades have seen a veritable explosion in the use of gold (I) complexes
bearing N-heterocyclic carbene (NHC) and phosphine (PR3) ligands. Both ligand families …
bearing N-heterocyclic carbene (NHC) and phosphine (PR3) ligands. Both ligand families …
Generation of donor/donor copper carbenes through copper-catalyzed diyne cyclization: enantioselective and divergent synthesis of chiral polycyclic pyrroles
FL Hong, ZS Wang, DD Wei, TY Zhai… - Journal of the …, 2019 - ACS Publications
The generation of metal carbenes from readily available alkynes represents a significant
advance in metal carbene chemistry. However, most of these transformations are based on …
advance in metal carbene chemistry. However, most of these transformations are based on …
Isoindolinone Synthesis via One‐Pot Type Transition Metal Catalyzed C− C Bond Forming Reactions
R Savela, C Méndez‐Gálvez - Chemistry–A European Journal, 2021 - Wiley Online Library
Isoindolinone structure is an important privileged scaffold found in a large variety of naturally
occurring as well as synthetic, biologically and pharmaceutically active compounds. Owing …
occurring as well as synthetic, biologically and pharmaceutically active compounds. Owing …
Gold-catalyzed homogeneous (cyclo) isomerization reactions
Gold is currently one of the most used metals in organometallic catalysis. The ability of gold
to activate unsaturated groups in different modes, together with its tolerance to a wide range …
to activate unsaturated groups in different modes, together with its tolerance to a wide range …
Gold-or Indium-Catalyzed Cross-Coupling of Bromoalkynes with Allylsilanes through a Concealed Rearrangement
ME de Orbe, M Zanini, O Quinonero… - ACS …, 2019 - ACS Publications
The gold (I)-catalyzed reaction of bromoalkynes with allylsilanes gives 1, 4-enynes in a
formal cross-coupling reaction. Mechanistic studies revealed the involvement of gold (I) …
formal cross-coupling reaction. Mechanistic studies revealed the involvement of gold (I) …
Catalyst-controlled site-selective N–H and C3-arylation of carbazole via carbene transfer reactions
A site-selective direct arylation reaction of carbazole and other N-heterocycles with diazo-
naphthalen-2 (1H)-ones has been developed. While Au (I)-NHC catalysts lead to selective …
naphthalen-2 (1H)-ones has been developed. While Au (I)-NHC catalysts lead to selective …
Mild Catalyst-and Additive-Free Three-Component Synthesis of 3-Thioisoindolinones and Tricyclic γ-Lactams Accelerated by Microdroplet Chemistry
C Dai, C Huang, M Ye, J Liu… - The Journal of Organic …, 2024 - ACS Publications
Isoindolinones, bearing both γ-lactam and aromatic rings, draw extensive interest in organic,
pharmaceutical, and medicinal communities as they are important structural motifs in many …
pharmaceutical, and medicinal communities as they are important structural motifs in many …
Hetero-Tetradehydro-Diels–Alder Cycloaddition of Enynamides and Cyanamides: Gold-Catalyzed Generation of Diversely Substituted 2, 6-Diaminopyridines
NV Shcherbakov, DV Dar'in… - The Journal of …, 2021 - ACS Publications
Gold (I)-catalyzed hetero-tetradehydro-Diels–Alder cycloaddition of enynamides and
cyanamides comprises an efficient route to diversely substituted 2, 6-diaminopyridines (28 …
cyanamides comprises an efficient route to diversely substituted 2, 6-diaminopyridines (28 …
Intramolecular activation of strong Si–O bonds by gold (i): regioselective synthesis of 3-bromo-2-silylbenzofurans
P Fernández-Canelas, R Miguélez, E Rubio… - Chemical …, 2022 - pubs.rsc.org
The high reactivity of gold-vinylidene complexes, generated in situ by [1, 2]-bromine shift
from the corresponding 1-bromoalkynes, allows the activation of one of the strongest bonds …
from the corresponding 1-bromoalkynes, allows the activation of one of the strongest bonds …