[HTML][HTML] Dimethyl acetylenedicarboxylate: A versatile tool in organic synthesis

CG Neochoritis, T Zarganes-Tzitzikas… - …, 2014 - thieme-connect.com
This review presents the recent progress in the chemistry of dimethyl acetylenedicarboxylate
(DMAD). The interest in and applications of this powerful reagent with more than 135 years …

The vital use of isocyanide-based multicomponent reactions (MCR) in chemical synthesis

RL Mohlala, EM Coyanis - Physical Sciences Reviews, 2024 - degruyter.com
Multicomponent (MCRs) reactions are classified as one-pot reaction where more than two
starting materials are employed to form a single product that contains the building blocks of …

Metal-free synthesis of quinoline-2, 4-dicarboxylate derivatives using aryl amines and acetylenedicarboxylates through a pseudo three-component reaction

S Ali, AT Khan - Organic & Biomolecular Chemistry, 2021 - pubs.rsc.org
An efficient, useful and one-pot protocol for the synthesis of quinoline-2, 4-dicarboxylate
scaffolds is accomplished from aryl amines and dimethyl/diethyl acetylenedicarboxylates …

Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and-selones

KV Belyaeva, LV Andriyankova, LP Nikitina… - Tetrahedron, 2014 - Elsevier
The three-component reaction of 1-substituted imidazoles, cyanophenylacetylene, and
elemental sulfur or selenium proceeds readily (for sulfur at room temperature without …

Metal-Free One-Pot Chemoselective thiocyanation of imidazothiazoles and 2-aminothiazoles with in situ generated N-thiocyanatosuccinimide

SN Kadam, AN Ambhore, MJ Hebade, RD Kamble… - Synlett, 2018 - thieme-connect.com
A chemoselective thiocyanation of imidazothiazoles and 2-aminothiazoles with use of in situ
generated N-thiocyanatosuccinimide (NTS) at room temperature is described. The protocol …

Synthetic access to imidazo[2,1-b]thiazoles

HA Mohamed, BF Abdel-Wahab - Journal of Sulfur Chemistry, 2012 - Taylor & Francis
Full article: Synthetic access to imidazo[2,1-b]thiazoles Skip to Main Content Taylor and Francis
Online homepage Taylor and Francis Online homepage Log in | Register Cart 1.Home 2.All …

Three‐Step One‐Pot Synthesis of Imidazo[2,1‐b]chalcogenazoles via Intramolecular Cyclization of N‐Alkynylimidazoles

JA Roehrs, RP Pistoia, DF Back… - Advanced Synthesis & …, 2012 - Wiley Online Library
Imidazo‐chalcogenazoles are easily accessible from the corresponding N‐
alkynylimidazoles by a three‐step, one‐pot chalcogenation reaction. The generality of this …

Ionic‐liquid‐promoted Four‐component One‐pot Synthesis of Highly Functionalized Benzimidazo[2,1‐b][1,3]thiazines: Facile Construction of N‐fused Heterocycles

IR Siddiqui, A Srivastava, S Shamim… - Asian Journal of …, 2013 - Wiley Online Library
A one‐pot, four‐component, efficient, and facile synthesis of highly functionalized
benzimidazo [2, 1‐b][1, 3] thiazines promoted by ionic liquid ([bmim] Br)/Et3N has been …

Azodicarboxylates: valuable reagents for the multicomponent synthesis of novel 1, 3, 4-thiadiazoles and imidazo [2, 1-b][1, 3, 4] thiadiazoles

T Zarganes-Tzitzikas, CG Neochoritis… - Tetrahedron, 2013 - Elsevier
Upon reaction of 4, 5-disubstituted-N-arylaminoimidazole-2-thiones with isocyanides in the
presence of azodicarboxylates (1.2 equiv) at rt, the imidazo [2, 1-b][1, 3, 4] thiadiazoles were …

Heterocycles from the reaction of thione groups with acetylenic bonds

AA Aly, AB Brown, AA Hassan - Advances in Heterocyclic Chemistry, 2014 - Elsevier
This chapter discusses reactions between the thione and alkyne functional groups,
subdivided into internal (intramolecular) and external (intermolecular) reactions. Many such …