Results 11 to 20 of about 2,043,921 (203)

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

open access: yesOrganic Letters, 2017
The Ugi four-component reaction (U-4CR) with N-hydroxyimides as a novel carboxylic acid isostere has been reported. This reaction provides straightforward access to α-hydrazino amides.
Ajay L Chandgude, Alexander Domling
exaly   +5 more sources

Catalytic Three‐Component Ugi Reaction [PDF]

open access: yesAngewandte Chemie International Edition, 2008
Perfect atom economy characterizes a novel catalytic three‐component Ugi reaction (see example). Different α‐amino amides are formed in good yields from aldehydes, primary amines, and isocyanides in the presence of phenyl phosphinic acid as the catalyst. The products will be useful for the synthesis of α‐amino acid derivatives and in diversity‐oriented
Pan, S., List, B.
openaire   +4 more sources

Diastereoselective Ugi reaction for the synthesis of unnatural amino esters

open access: yesOrbital: The Electronic Journal of Chemistry, 2012
Multicomponent Reactions (MCR) are useful reactions to obtain complex products by the simple mixture of 3 or more reactants. The classic Ugi reaction (4-UCR) involves a mixture of an amine, aldehyde, isocyanide and a carboxylic acid, giving peptoides as ...
Rafael Oliveira Rocha   +4 more
doaj   +2 more sources

DFT Studies on the Stereoselective Three-Component Ugi Reaction [PDF]

open access: yesOrbital: The Electronic Journal of Chemistry, 2019
Mechanism and stereochemistry of three component Ugi reaction (3C-Ugi) were studied theoretically based on DFT calculations. Structures of reagents, products, intermediates, and transition states were optimized at M062X/6-31+g(d,p) level of theory in gas
Elaheh Sadat Sharifzadeh   +1 more
doaj   +4 more sources

Novel postmodifications of the Ugi reaction [PDF]

open access: yes, 2016
In this thesis several novel postmodifiactions of regular Ugi-4CR products have been examined. Their scope and limitations were tested both by permutating the required functionalities around the Ugi scaffold and by synthesizing compound libraries for successful permutations. The following reactions were examined: 1.
Welsch, Sebastian
openaire   +3 more sources

New tandem Ugi/intramolecular Diels–Alder reaction based on vinylfuran and 1,3-butadienylfuran derivatives

open access: yesBeilstein Journal of Organic Chemistry
A new tandem sequence involving the Ugi reaction and Diels–Alder [4 + 2] cycloaddition based on vinylfuran and 1,3-butadienylfuran derivatives was designed and studied.
Yuriy I. Horak   +5 more
doaj   +2 more sources

Innovations and Inventions: Why Was the Ugi Reaction Discovered Only 37 Years after the Passerini Reaction? [PDF]

open access: yesJ Org Chem, 2023
This year represents the 100th anniversary of the discovery of the Passerini three-component reaction. The related Ugi four-compound reaction was discovered 37 years after the Passerini reaction.
Dömling A.
europepmc   +3 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

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics. [PDF]

open access: yesOrg Lett, 2017
A general strategy is introduced for the efficient synthetic access of disulfide linked artificial macrocycles via a Ugi four-component reaction (U4CR) followed by oxidative cyclization.
Vishwanatha TM   +2 more
europepmc   +3 more sources

Two-Step Macrocycle Synthesis by Classical Ugi Reaction [PDF]

open access: yesJournal of Organic Chemistry, 2018
Shabnam Shaabani   +2 more
exaly   +2 more sources

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