Results 31 to 40 of about 4,769 (209)

Synthesis of Boron-Containing Primary Amines

open access: yesMolecules, 2013
In this study, boron-containing primary amines were synthesized for use as building blocks in the study of peptoids. In the first step, Gabriel synthesis conditions were modified to enable the construction of seven different aminomethylphenyl boronate ...
Sheng-Hsuan Chung   +4 more
doaj   +1 more source

The Ugi-Smiles Reaction on Steroids: Discovery of Bioactive N,N-Disubstituted 3- Aminoestrones

open access: yes, 2020
The Ugi-Smiles multicomponent reaction is a powerful tool for obtaining N-arylamines from acidic phenols and has been widely used for gaining access to structurally diverse scaffolds. In this work we demonstrate that this isocyanide-based coupling can be
Evelyn, Bonifazi   +5 more
core   +1 more source

Ugi Multicomponent Reaction Based Synthesis of Medium-Sized Rings [PDF]

open access: yes, 2017
An Ugi multicomponent reaction based two-step strategy was applied to generate medium-sized rings. In the first linear expansion phase, a series of diamines reacted with cyclic anhydrides to produce different lengths of terminal synthetic amino acids as ...
Eman M. M. Abdelraheem   +14 more
core   +3 more sources

Long-range diastereoselectivity in Ugi reactions of 2-substituted dihydrobenzoxazepines

open access: yesBeilstein Journal of Organic Chemistry, 2011
The Ugi reaction of 2-substituted dihydrobenzoxazepines was found to proceed with unexpectedly good diastereoselectivitiy (diastereoisomeric ratios up to 9:1), despite the large distance between the pre-existing stereogenic centre and the newly generated
Luca Banfi   +4 more
doaj   +1 more source

Diverse Isoquinoline Scaffolds by Ugi/Pomeranz–Fritsch and Ugi/Schlittler–Müller Reactions [PDF]

open access: yesOrganic Letters, 2019
The Pomeranz-Fritsch reaction and its Schlittler-Müller modification were successfully applied in the Ugi postcyclization strategy by using orthogonally protected aminoacetaldehyde diethyl acetal and complementary electron rich building blocks. Several scaffolds, including isoquinolines, carboline, alkaloid-like tetrazole-fused tetracyclic compounds ...
Yuanze Wang   +4 more
openaire   +3 more sources

'Atypical Ugi' tetrazoles [PDF]

open access: yes, 2020
Amino acid-derived isocyano amides together with TMSN3, oxocomponents and 1° or 2° amines are common substrates in the Ugi tetrazole reaction. We surprisingly found that combining these substrates gives two different constitutional isomeric Ugi products ...
Abdelraheem, Eman M M   +8 more
core   +1 more source

Oxa-Michael/Ugi-Smiles cascade reaction with α,β-unsaturated aldehydes

open access: yesResults in Chemistry, 2022
Use of α,β-unsaturated aldehydes as components in Ugi-Smiles couplings of 2-nitrophenol with alkyl isocyanides and primary amines provides ready access to γ-alkoxy substituted amides when performed in the presence of alcoholic solvents. The observed five
Aubrey Thessing   +5 more
doaj   +1 more source

Synthesis of Novel Diterpenic Peptides via the Ugi Reaction and Their Anticancer Activities

open access: yesMolbank, 2023
Novel diterpenic peptide derivatives were synthesized via the Ugi four-component reaction at ambient temperature. The protocol employed a reaction between formaldehyde, benzyl amine, the corresponding diterpene acid, and ethyl 2-isocyanoacetate.
Anna A. Smirnova   +3 more
doaj   +1 more source

Direct synthesis of the arylboronic acid analogues of phenylglycine via microwave-assisted four-component Ugi reaction

open access: yes, 2014
A four-component Ugi reaction (Ugi-4CR) utilizing formylphenyl boronic acids under mild condition was developed for the synthesis of arylboronic acid analogs.
Lian, Ru-Ching; Lin, Meng-Hsuan; Liao, Pin-Hsuan; Fu, Jia-Jie; Wu, Meng-Ju; Wu, Yang-Chang; Chang, Fang-Rong; Wu, Chin-Chung; Pan, Po-Shen   +1 more
core   +1 more source

Synthesis of Chromeno[3,4-b]piperazines by an Enol-Ugi/Reduction/Cyclization Sequence

open access: yesMolecules, 2021
Keto piperazines and aminocoumarins are privileged building blocks for the construction of geometrically constrained peptides and therefore valuable structures in drug discovery.
Ana Bornadiego   +2 more
doaj   +1 more source

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