3-Acyltetramic acids as a novel class of inhibitors for human kallikreins 5 and 7

AS de Souza, BDC Pacheco, S Pinheiro… - Bioorganic & medicinal …, 2019 - Elsevier
Abstract Human kallikreins 5 and 7 (KLK5 and KLK7) exhibit trypsin-and chymotrypsin-like
activities and are involved in pathologies related to skin desquamation process. A series of …

Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro)

PHRA Azevedo, PG Camargo, LEC Constant… - Scientific Reports, 2024 - nature.com
COVID-19 is a multisystemic disease caused by the SARS-CoV-2 airborne virus, a member
of the Coronaviridae family. It has a positive sense single-stranded RNA genome and …

Nucleophilic ring-opening of epoxide and aziridine acetates for the stereodivergent synthesis of β-hydroxy and β-amino γ-lactams

TB Bisol, AJ Bortoluzzi, MM Sa - The Journal of Organic Chemistry, 2011 - ACS Publications
A highly regio-and stereoselective synthesis of novel β, γ-disubstituted γ-lactams with either
an anti or syn relative configuration was developed from readily available epoxide and …

Copper catalyzed oxidative cross-coupling of aromatic amines with 2-pyrrolidinone: A facile synthesis of N-aryl-γ-amino-γ-lactams

S Priyadarshini, PJA Joseph, ML Kantam - Tetrahedron, 2014 - Elsevier
Copper catalyzed oxidative cross-coupling of aromatic amines with 2-pyrrolidinone: a facile
synthesis of N-aryl-γ-amino-γ-lactams - ScienceDirect Skip to main contentSkip to article …

De Novo Synthesis of 3-Pyrrolin-2-Ones

ET Pelkey, SJ Pelkey, JG Greger - Advances in Heterocyclic Chemistry, 2015 - Elsevier
This review presents a systematic survey of the literature (through the end of 2014) for de
novo syntheses of 3-pyrrolin-2-ones from acyclic precursors or via transformation of other …

Methodology for Synthesis of Enantiopure 3, 5‐Disubstituted Pyrrol‐2‐ones

O Krenk, J Kratochvíl, M Špulák… - European Journal of …, 2015 - Wiley Online Library
A new synthetic route towards chiral 3, 5‐disubstituted pyrrol‐2‐ones by starting from amino
acids has been developed. The sequence features the conversion of amino acids into their …

Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, allo-Threonine, and Cysteine

H Bagum, KE Christensen, M Genov… - The Journal of …, 2019 - ACS Publications
A general route which provides direct access to pyroglutamates from tetramates, making use
of Suzuki coupling on an enol mesylate, followed by reduction, is reported. This work permits …

Conjugate addition of amines to chiral 3-aziridin-2-yl-acrylates

DH Yoon, HJ Ha, BC Kim, WK Lee - Tetrahedron Letters, 2010 - Elsevier
Conjugate addition of benzylamine to chiral methyl cis-3-aziridin-2-yl-acrylates was
successfully proceeded to yield 3-aziridin-2-yl-3-benzylaminopropionates in high yield with …

[HTML][HTML] Efficient synthesis of new 1-alkyl (aryl)-5-(3, 3, 3-trihalo-2-oxopropylidene)-1H-pyrrol-2 (5H)-ones

AFC Flores, L Pizzuti, LA Piovesan, DC Flores… - Tetrahedron …, 2010 - Elsevier
The synthesis of 1-alkyl (aryl)-5-(3, 3, 3-trihalo-2-oxopropylidene)-1H-pyrrol-2 (5H)-ones 5,
6a–d from 1-alkyl (aryl)-4-bromo-5-(3, 3, 3-trihalo-2-oxopropylidene)-1H-pyrrolidin-2-ones 3 …

Access to β, γ-diamino acids. Application to the synthesis of 3-deoxyaminostatine

F Bouillère, R Guillot, C Kouklovsky… - Organic & Biomolecular …, 2011 - pubs.rsc.org
Access to β,γ-diamino acids. Application to the synthesis of 3-deoxyaminostatine - Organic
& Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C0OB00370K Royal Society of …