Tetrazoles via multicomponent reactions

CG Neochoritis, T Zhao, A Domling - Chemical reviews, 2019 - ACS Publications
Tetrazole derivatives are a prime class of heterocycles, very important to medicinal
chemistry and drug design due to not only their bioisosterism to carboxylic acid and amide …

Synthesis of polyheterocycles via multicomponent reactions

IA Ibarra, A Islas-Jácome… - Organic & Biomolecular …, 2018 - pubs.rsc.org
Polyheterocycles are one of the most desired synthetic targets due to their numerous and
valuable applications in various fields. Multicomponent reactions (MCRs) are highly …

The Ugi three-component reaction and its variants

JC Flores-Reyes, A Islas-Jácome… - Organic Chemistry …, 2021 - pubs.rsc.org
More than 60 years have passed since I. Ugi synthesized the first α-amidoamides in one
experimental step involving a combination of aldehydes, amines, carboxylic acids and …

Synthesis of bis-furyl-pyrrolo [3, 4-b] pyridin-5-ones via Ugi–Zhu reaction and in vitro activity assays against human SARS-CoV-2 and in silico studies on its main …

I Morales-Salazar, FP Montes-Enríquez… - RSC Medicinal …, 2023 - pubs.rsc.org
An Ugi–Zhu three-component reaction (UZ-3CR) coupled in one pot manner to a cascade
process (N-acylation/aza Diels–Alder cycloaddition/decarboxylation/dehydration) was …

The Pictet–Spengler Reaction: A Powerful Strategy for the Synthesis of Heterocycles

P Gholamzadeh - Advances in Heterocyclic Chemistry, 2019 - Elsevier
Abstract Ever since Amé Pictet and Theodor Spengler discovered their way to synthesize
tetrahydroisoquinolines and β-carbolines, their method became a powerful methodology for …

Synthesis of tris-heterocycles via a cascade IMCR/aza Diels-Alder+ CuAAC strategy

MA Rentería-Gómez, A Islas-Jácome… - Frontiers in …, 2019 - frontiersin.org
6-Triazolylmethyl-pyrrolo [3, 4-b] pyridin-5-one tris-heterocycles were synthesized in 43–
57% overall yields. The two-stage synthesis involved a cascade process (Ugi-3CR/aza Diels …

Propargylation of Ugi amide dianion: an entry into pyrrolidinone and benzoindolizidine alkaloid analogues

A Zidan, M Cordier, AM El-Naggar… - Organic …, 2018 - ACS Publications
Propargylation of Ugi adducts under the addition of excess sodium hydride in DMSO leads
to direct formation of pyrrolidinone enamides, which are useful precursors of iminium …

Synthesis of 2-Tetrazolylmethyl-isoindolin-1-ones via a One-Pot Ugi-Azide/(N-Acylation/exo-Diels–Alder)/Dehydration Process

A Rentería-Gómez, A Islas-Jácome… - ACS …, 2016 - ACS Publications
A series of fifteen 2-tetrazolylmethyl-isoindolin-1-one linked-type bis-heterocycles were
synthesized in 10–76% yields under mild conditions via a one-pot Ugi-azide/(N …

Ultrasound-assisted diastereoselective green synthesis of spiro-fused-γ-lactams functionalized with an amide bond heterocyclic bioisostere via the Ugi azide/domino …

D Calderón-Rangel, Á Rentería-Gómez… - Organic & …, 2024 - pubs.rsc.org
A series of linked-type 1, 5-disubstituted tetrazoles (1, 5-DS-Ts) were synthesised via an
isocyanide-based multicomponent reaction (IMCR) and used as synthetic platforms to …

Synthesis of Pyrrolo[3,4-b]pyridin-5-ones via Multicomponent Reactions and In Vitro–In Silico Studies Against SiHa, HeLa, and CaSki Human Cervical Carcinoma …

D Segura-Olvera, AN García-González… - Molecules, 2019 - mdpi.com
A series of 12 polysubstituted pyrrolo [3, 4-b] pyridin-5-ones were synthesized via a one-pot
cascade process (Ugi–3CR/aza Diels-Alder/N-acylation/decarboxylation/dehydration) and …