Indole-based derivatives as potential antibacterial activity against methicillin-resistance Staphylococcus aureus (MRSA)

HL Qin, J Liu, WY Fang, L Ravindar… - European journal of …, 2020 - Elsevier
Antibacterial-resistance speaks to an overall alarm, particularly in regards to the flare-up of
methicillin-resistance Staphylococcus aureus (MRSA), a classic reason for genuine skin and …

Metal-mediated and metal-catalyzed reactions under mechanochemical conditions

A Porcheddu, E Colacino, L De Luca, F Delogu - ACS Catalysis, 2020 - ACS Publications
The extraordinary impact of metal-based complexes on synthetic methods is still recognized
nowadays, and attempts are currently undertaken to further extend the use of metal-assisted …

Transition metal-catalyzed C–H functionalizations of indoles

P Kumar, PJ Nagtilak, M Kapur - New Journal of Chemistry, 2021 - pubs.rsc.org
Over the last two decades, transition-metal catalyzed C–H functionalization of indoles has
emerged as an area of extensive research and tremendous progress has been made in this …

Indole-2-carboxylic acid derived mono and bis 1, 4-disubstituted 1, 2, 3-triazoles: Synthesis, characterization and evaluation of anticancer, antibacterial, and DNA …

S Narsimha, NS Kumar, BK Swamy, NV Reddy… - Bioorganic & medicinal …, 2016 - Elsevier
A series of new indole-2-carboxylic acid derived mono and bis 1, 4-disubstituted 1, 2, 3
triazoles (I 1–I 6 and I 7–I 12) were synthesized and screened for their anticancer (in vitro …

Regioselective C3Alkylation of Indoles for the Synthesis of Bis(indolyl)methanes and 3-Styryl Indoles

R Zhang, R Ma, R Chen, L Wang… - The Journal of Organic …, 2024 - ACS Publications
Herein, we describe an efficient transition-metal-free regioselective C3alkylation of indoles
for the synthesis of bis (indolyl) methanes and 3-styryl indoles. Nitrobenzene is employed as …

Chiral Anion Phase Transfer of Aryldiazonium Cations: An Enantioselective Synthesis of C3‐Diazenated Pyrroloindolines

HM Nelson, SH Reisberg… - Angewandte Chemie …, 2014 - Wiley Online Library
Herein is reported the first asymmetric utilization of aryldiazonium cations as a source of
electrophilic nitrogen. This is achieved through a chiral anion phase‐transfer …

Mild and selective base-free C–H arylation of heteroarenes: experiment and computation

HPL Gemoets, I Kalvet, AV Nyuchev, N Erdmann… - Chemical …, 2017 - pubs.rsc.org
A mild and selective C–H arylation strategy for indoles, benzofurans and benzothiophenes
is described. The arylation method engages aryldiazonium salts as arylating reagents in …

Dual vicinal functionalisation of heterocycles via an interrupted Pummerer coupling/[3, 3]-sigmatropic rearrangement cascade

M Šiaučiulis, S Sapmaz, AP Pulis, DJ Procter - Chemical Science, 2018 - pubs.rsc.org
A dual vicinal functionalisation cascade involving the union of heterocycles and allyl
sulfoxides is described. In particular, the approach provides efficient one-step access to …

Ruthenium-catalyzed heteroatom-directed regioselective C–H arylation of indoles using a removable tether

VK Tiwari, N Kamal, M Kapur - Organic letters, 2015 - ACS Publications
A new approach to C-2 arylated indoles has been developed by utilizing a ruthenium-
catalyzed, heteroatom-directed regioselective C–H arylation. The reaction is highly site …

Aryldiazonium-Salt-Triggered Carboxylative Azotization of Pyrroles or Indoles with Polyhalomethanes via Halogen-Atom Transfer (XAT)

TB Zhang, F Wang, JY Ouyang, ZW Luo, JH Qin… - Organic …, 2024 - ACS Publications
A halogen-atom-transfer (XAT)-based method for carbonylazotization of pyrroles or indoles
with aryldiazonium salts and polyhalomethanes via dual C (sp2)–H bond functionalization is …