Results 1 to 10 of about 2,988 (132)

Harnessing unprotected deactivated amines and arylglyoxals in the Ugi reaction for the synthesis of fused complex nitrogen heterocycles [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Piperazines and diazepines are examples of nitrogen heterocycles present in many marketed drugs highlighting their importance in the discovery of novel bioactive compounds.
Javier Gómez-Ayuso   +5 more
doaj   +2 more sources

Sequential Ugi reaction/base-induced ring closing/IAAC protocol toward triazolobenzodiazepine-fused diketopiperazines and hydantoins [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2018
A practical three-step protocol for the assembly of triazolobenzodiazepine-fused diketopiperazines and hydantoins has been developed. The synthesis of these tetracyclic ring systems was initiated by an Ugi reaction, which brought together all necessary ...
Robby Vroemans   +7 more
doaj   +2 more sources

α-Ketoglutaric acid in Ugi reactions and Ugi/aza-Wittig tandem reactions [PDF]

open access: yesBeilstein Journal of Organic Chemistry
A small library of bis- and tetraamides was synthesized by the Ugi reaction with α-ketoglutaric acid, tert-butyl isocyanide, aromatic aldehydes, and aromatic amines.
Vladyslav O. Honcharov   +6 more
doaj   +2 more sources

Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2016
Enantiomerically pure β-aminoalcohols, produced through an organocatalytic Mannich reaction, were subjected to an Ugi multicomponent reaction under classical or Lewis acid-promoted conditions with diastereoselectivities ranging from moderate to good ...
Samantha Caputo   +5 more
doaj   +2 more sources

N-Hydroxyimide Ugi Reaction toward α-Hydrazino Amides [PDF]

open access: yesOrganic Letters, 2017
Ajay L Chandgude, Alexander Domling
exaly   +2 more sources

Ammonia-Promoted One-Pot Tetrazolopiperidinone Synthesis by Ugi Reaction [PDF]

open access: yesACS Combinatorial Science, 2017
Justyna Kalinowska-Tłuścik   +2 more
exaly   +2 more sources

Propargyl Amines: Versatile Building Blocks in Post‐Ugi Transformations

open access: yesChemistryOpen, 2023
The Ugi reaction, a multicomponent reaction, allows diversity‐oriented synthesis Its importance is recognized by an exponential increase in the publications utilizing the post‐Ugi transformations as a strategy to build complex molecules via simple and ...
Rinkal B. Bhoraniya, Dr. Sachin G. Modha
doaj   +1 more source

Ugi Four-Component Reactions Using Alternative Reactants

open access: yesMolecules, 2023
The Ugi four-component reaction (Ugi-4CR) undoubtedly is the most prominent multicomponent reaction (MCRs) that has sparked organic chemists’ interest in the field.
Seyyed Emad Hooshmand, Wei Zhang
doaj   +1 more source

Strain and Complexity, Passerini and Ugi Reactions of Four‐Membered Heterocycles and Further Elaboration of TOSMIC Product

open access: yesChemistryOpen, 2023
Straightforward and general Passerini and Ugi procedures have been developed to incorporate four‐membered heterocycles into highly functionalized scaffolds.
Gábor Sztanó   +2 more
doaj   +1 more source

Controlling the stereochemistry in 2-oxo-aldehyde-derived Ugi adducts through the cinchona alkaloid-promoted electrophilic fluorination

open access: yesBeilstein Journal of Organic Chemistry, 2020
In this report, we introduce a new strategy for controlling the stereochemistry in Ugi adducts. Instead of controlling stereochemistry directly during the Ugi reaction we have attempted to stereodefine the chiral center at the peptidyl position through ...
Yuqing Wang   +9 more
doaj   +1 more source

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