Results 41 to 50 of about 27,319 (289)

Photothermal conversion triggered thermal asymmetric catalysis within metal nanoparticles loaded homochiral covalent organic framework

open access: yesNature Communications, 2019
Achieving both high stereoselectivity and yield is a challenge for conventional asymmetric catalysis. Here, the authors report two metal nanoparticle-loaded and porphyrin-containing homochiral covalent organic framework-based composite catalysts that ...
Hui-Chao Ma   +3 more
doaj   +1 more source

The Stereoselectivity of Drug Action [PDF]

open access: yesPharmacology & Toxicology, 1989
Pharmacologists and toxicologists are in the midst of demonstrating the importance of spatial (three-dimensional) molecular features in the functions of biological systems and in the therapeutic actions and side effects of drugs. Recent findings indicate that spatial features in a variety of biologically active molecules play a decisive role in many ...
openaire   +2 more sources

Synthesis and 1,3-Dipolar Cycloaddition Reactions of Chiral Maleimides

open access: yesMolecules, 1997
New routes to the synthesis of various novel chiral maleimides are described. The oxabicyclic anhydride 2 readily available exo-Diels-Alder adduct of furan and maleic anhydride was used as a vehicle, which in turn reacted with hydrochlorides of amino ...
Lubor Fisera, Vladimir Ondrus
doaj   +1 more source

Recent Advances of Pharmaceutical Process Chemistry and Its Innovation in China: Part 1

open access: yesPharmaceutical Fronts, 2020
This review article summarizes recent developments and innovations in China's pharmaceutical process chemistry over the last several decades. Case studies of dozens of blockbuster drug processes are presented, including bulk drugs, such as the over-the ...
Pei Tang   +5 more
doaj   +1 more source

The Origin of Stereoselectivity in the Hydrogenation of Oximes Catalyzed by Iridium Complexes: A DFT Mechanistic Study

open access: yesMolecules, 2022
Herein the reaction mechanism and the origin of stereoselectivity of asymmetric hydrogenation of oximes to hydroxylamines catalyzed by the cyclometalated iridium (III) complexes with chiral substituted single cyclopentadienyl ligands (Ir catalysts A1 and
Qaim Ali   +6 more
doaj   +1 more source

Stereoselectivity of the Thia-Sommelet [2,3]-Dearomatization

open access: yes, 2016
Stereoselectivity of the Thia-Sommelet [2,3 ...
Richard Berger (1417021)   +2 more
core   +2 more sources

Application of Chiral Transfer Reagents to Improve Stereoselectivity and Yields in the Synthesis of the Anti-Tuberculosis Drug Bedaquiline

open access: yes, 2023
Bedaquiline (BDQ) is an important drug for treating multidrug-resistant tuberculosis (MDR-TB), a worldwide disease that causes more than 1.6 million deaths yearly.
Gopal, Sirasani   +14 more
core   +1 more source

Synthesis of Glycosides of Glucuronic, Galacturonic and Mannuronic Acids: An Overview

open access: yesMolecules, 2011
Uronic acids are carbohydrates present in relevant biologically active compounds. Most of the latter are glycosides or oligosaccharides linked by their anomeric carbon, so their synthesis requires glycoside-bond formation. The activation of this anomeric
José Kovensky, Anne Wadouachi
doaj   +1 more source

Implications of Pharmacokinetic Potentials of Pioglitazone Enantiomers in Rat Plasma Mediated through Glucose Uptake Assay

open access: yesMolecules, 2023
Pioglitazone, a PPAR-gamma activator used to diagnose hyperglycemia, was studied for its stereoselective deposition and active enantiomers in female albino Wistar rats.
Tatineni Spandana   +8 more
doaj   +1 more source

A stereoselective synthesis of (+)-boronolide [PDF]

open access: yesTetrahedron Letters, 2000
A stereoselective synthesis of (+)-boronolide is described. The key steps involve a stereoselective reduction of an α-hydroxy ketone, allylation of an α-hydroxy aldehyde and a ring-closing olefin metathesis of a homoallylic alcohol derived acrylate ester utilizing Grubbs' catalyst.
Arun K, Ghosh, Geoffrey, Bilcer
openaire   +2 more sources

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