A review on DBU-mediated organic transformations
SK Boddu, N Ur Rehman, TK Mohanta… - … Chemistry Letters and …, 2022 - Taylor & Francis
Diazabicyclo [5.4. 0] undec-7-ene (DBU) has received a significant importance in organic
synthesis during recent years because of its interesting ability to catalyze organic reaction …
synthesis during recent years because of its interesting ability to catalyze organic reaction …
Ultrasound-assisted synthesis of heterocyclic compounds
In this review, we tried to underscore the synthesis of the heterocyclic compounds under
assisted ultrasonic irradiation. The ultrasonic irradiation has been applied for medicinal …
assisted ultrasonic irradiation. The ultrasonic irradiation has been applied for medicinal …
An Organocatalytic Azide–Aldehyde [3+ 2] Cycloaddition: High‐Yielding Regioselective Synthesis of 1, 4‐Disubstituted 1, 2, 3‐Triazoles
DB Ramachary, AB Shashank… - Angewandte Chemie …, 2014 - Wiley Online Library
Abstract An organocatalytic azide–aldehyde [3+ 2] cycloaddition (organo‐click) reaction of a
variety of enolizable aldehydes is reported. The organo‐click reaction is characterized by a …
variety of enolizable aldehydes is reported. The organo‐click reaction is characterized by a …
Ultrasound promoted one pot synthesis of novel fluorescent triazolyl spirocyclic oxindoles using DBU based task specific ionic liquids and their antimicrobial activity
Spirocyclic oxindoles and triazolyl derivatives posses remarkable biological activities. In
present work, we have described an efficient one pot four-component domino reaction of 1 …
present work, we have described an efficient one pot four-component domino reaction of 1 …
An efficient one-pot strategy for the highly regioselective metal-free synthesis of 1, 4-disubstituted-1, 2, 3-triazoles
A simple and efficient metal-free methodology for the regioselective synthesis of 1, 4-
disubstituted-1, 2, 3-triazoles has been developed by applying a novel inverse electron …
disubstituted-1, 2, 3-triazoles has been developed by applying a novel inverse electron …
Identification of 2-(N-aryl-1,2,3-triazol-4-yl) quinoline derivatives as antitubercular agents endowed with InhA inhibitory activity
A Sabt, MH Abdulla, MS Ebaid, J Pawełczyk… - Frontiers in …, 2024 - frontiersin.org
The spread of drug-resistant tuberculosis strains has become a significant economic burden
globally. To tackle this challenge, there is a need to develop new drugs that target specific …
globally. To tackle this challenge, there is a need to develop new drugs that target specific …
Discovery of new quinoline derivatives bearing 1-aryl-1, 2, 3-triazole motif as influenza H1N1 virus neuraminidase inhibitors
Sporadically and periodically, influenza outbreaks threaten global health and the economy.
Antigen drift-induced influenza virus mutations hamper antiviral drug development. Thus, a …
Antigen drift-induced influenza virus mutations hamper antiviral drug development. Thus, a …
Organocatalytic 1, 3-dipolar cycloaddition reaction of α, β-unsaturated ketones with azides through iminium catalysis
W Li, Z Du, K Zhang, J Wang - Green Chemistry, 2015 - pubs.rsc.org
Organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated ketones with azides
through iminium catalysis - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC01929F …
through iminium catalysis - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC01929F …
Thiol (-SH) substituent as functional motif for effective corrosion protection: A review on current advancements and future directions
Thiols are the compounds that contain–SH functional group in their molecular structures.
They are also called as sulfanyls, sulfhydryls or mercaptans. Generally, thiol based …
They are also called as sulfanyls, sulfhydryls or mercaptans. Generally, thiol based …
Azide–acetonitrile “click” reaction triggered by Cs 2 CO 3: The atom-economic, high-yielding synthesis of 5-amino-1, 2, 3-triazoles
PM Krishna, DB Ramachary, S Peesapati - RSC advances, 2015 - pubs.rsc.org
Azide–acetonitrile “click” reaction triggered by Cs 2 CO 3 : the atom-economic, high-yielding
synthesis of 5-amino-1,2,3-triazoles - RSC Advances (RSC Publishing) DOI:10.1039/C5RA12308A …
synthesis of 5-amino-1,2,3-triazoles - RSC Advances (RSC Publishing) DOI:10.1039/C5RA12308A …