Replacement strategies for non-green dipolar aprotic solvents

F Gao, R Bai, F Ferlin, L Vaccaro, M Li, Y Gu - Green Chemistry, 2020 - pubs.rsc.org
Dipolar aprotic solvents (DMSO, DMF, DMAc, NMP, etc.) have been widely used in organic
synthesis and pharmaceutical research because of their remarkable polarities and …

Development of the applications of palladium on charcoal in organic synthesis

X Liu, D Astruc - Advanced Synthesis & Catalysis, 2018 - Wiley Online Library
Palladium on charcoal (Pd/C) has lots of salient merits:(i) it is a cheap and commercial
source of palladium,(ii) it shows efficient catalytic activity even without ligands,(iii) as a …

Environmentally Friendly, Co-catalyst-Free Chemical Fixation of CO2 at Mild Conditions Using Dual-Walled Nitrogen-Rich Three-Dimensional Porous Metal–Organic …

B Ugale, S Kumar, TJ Dhilip Kumar… - Inorganic …, 2019 - ACS Publications
Highly porous, polyhedral metal–organic frameworks (MOFs) of Co (II)/Ni (II),{[M6 (TATAB) 4
(DABCO) 3 (H2O) 3]· 12DMF· 9H2O} n (where M= Co (II)(1)/Ni (II)(2), H3TATAB= 4, 4′, 4 …

A novel zirconium-based metal–organic framework covalently modified by methyl pyridinium bromide for mild and co-catalyst free conversion of CO 2 to cyclic …

JH Xu, SF Peng, YK Shi, S Ding, GS Yang… - Dalton …, 2023 - pubs.rsc.org
Building metal–organic frameworks (MOFs) covalently modified by onium halides is a
promising approach to develop efficient MOF-based heterogeneous catalysts for the …

Chemical Fixation of CO2 Under Solvent and Co-Catalyst-free Conditions Using a Highly Porous Two-fold Interpenetrated Cu(II)-Metal–Organic Framework

SS Dhankhar, R Das, B Ugale, RS Pillai… - Crystal Growth & …, 2021 - ACS Publications
A highly porous metal–organic framework (MOF) based on the Cu (II) ion,{[Cu6 (TATAB) 4
(DABCO) 3 (H2O) 3]· 24DMF} n (Cu (II)-MOF)(where H3TATAB= 4, 4′, 4 ″-s-triazine-1, 3, 5 …

Pd-Catalyzed Perfluoroalkylative Aryloxycarbonylation of Alkynes with Formates as CO Surrogates

B Gatlik, W Chaładaj - ACS Catalysis, 2021 - ACS Publications
The highly toxic, inflammable, and odorless nature of CO causes problematic handling on
laboratory-scale experiments. Replacement of CO cylinders by CO surrogates is particularly …

Carbonylative Tertiary Amide Synthesis from Aryl Iodides and Tertiary Amines via Oxidant‐Free C−N Bond Cleavage Catalyzed by Palladium(II) Chloride in …

RS Mane, BM Bhanage - Advanced Synthesis & Catalysis, 2017 - Wiley Online Library
In this work, we have described the carbonylative synthesis of amides from aryl iodides and
tertiary amines as an aminal source via oxidant‐free C (sp3)− N bond cleavage using in situ …

Palladium(II)/N-Heterocyclic Carbene-Catalyzed Direct C–H Acylation of Heteroarenes with N-Acylsaccharins

S Karthik, T Gandhi - Organic letters, 2017 - ACS Publications
N-Acylsaccharin represents a facile acyl group transfer agent to heteroarenes in the
presence of Pd (II)/NHC complexes appended with a pyrene unit. Catalytic acylation of …

Supported Palladium Catalyzed Carbonylative Coupling Reactions using Carbon Monoxide as C1 Source

Shaifali, Sheetal, P Das - The Chemical Record, 2022 - Wiley Online Library
The carbonylative reactions of aryl halides, boronic acids, amines, activated alkene and
alkynes under CO and supported palladium catalyzed conditions are very popular reactions …

Cu@UgC3N4 Catalyzed Cyclization of o-Phenylenediamines for the Synthesis of Benzimidazoles by Using CO2 and Dimethylamine Borane as a Hydrogen …

VV Phatake, BM Bhanage - Catalysis Letters, 2019 - Springer
This work reports a green and sustainable route for the synthesis of benzimidazoles via C–N
bond formation using carbon dioxide (CO 2) as a C 1 carbon source. In this work, Cu@ UgC …