Results 41 to 50 of about 62,467 (179)
Alternative pathways to α,β-unsaturated ketones via direct oxidative coupling transformation using Sr-doped LaCoO3 perovskite catalyst [PDF]
A strontium-doped lanthanum cobaltite perovskite material was prepared, and used as a recyclable and effective heterogeneous catalyst for the direct oxidative coupling of alkenes with aromatic aldehydes to produce α,β-unsaturated ketones.
Khang H. Trinh +7 more
doaj +1 more source
Asymmetric carbohydroxylation of alkenes offers an efficient approach to access chiral alcohols, a class of versatile building blocks in pharmaceutical and agrochemical industries, from abundant simple alkenes.
Yiyin Liu +7 more
doaj +1 more source
High chemoselectivity in the phenol synthesis
Efforts to trap early intermediates of the gold-catalyzed phenol synthesis failed. Neither inter- nor intramolecularly offered vinyl groups, ketones or alcohols were able to intercept the gold carbenoid species. This indicates that the competing steps of
Matthias Rudolph +3 more
doaj +1 more source
Pig Slurry Fertilization Changes the Pyrolytic Signature of Humic Substances in Calcareous Soil
The aim of this study was to determine the effect of progressive pig slurry (PS) rates, applied over a 12-year period, on the molecular composition of soil organic matter in a calcareous soil.
Àngela D. Bosch-Serra +3 more
doaj +1 more source
Inter- and intramolecular enantioselective carbolithiation reactions
In this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (−)-sparteine, to promote facial selection on a C=C bond.
Asier Gómez-SanJuan +2 more
doaj +1 more source
Homologative alkene difunctionalization
Abstract Systematic evaluation of homologous series plays a pivotal role in synthetic and medicinal chemistry 1,2 . Despite their structural resemblance, the preparation of homologs often requires individual synthetic planning tailored to distinct precursors and reactions.
Morgan Kim +5 more
openaire +2 more sources
Aminothiolation of alkenes with azoles and Bunte salts
We have developed an intermolecular aminothiolation of simple olefins using Bunte salt as a thiolating agent. This protocol produces thiyl free radicals under PIDA oxidation conditions, eliminating the need for transition-metal catalysts.
Bingqing Ouyang +4 more
doaj +1 more source
A Study of Alkene Disulfonoxylation
We have developed convenient protocols for alkene disulfonoxylation, which involve stirring alkene substrate with a commercial I(III) oxidant and sulfonic acid in CH2Cl2 at ambient temperature. The reactions can be performed open to air without any special precautions to exclude moisture and, in most cases, deliver the products of vicinal ...
Shyam Sathyamoorthi, Steven P. Kelley
openaire +2 more sources
Direct and site-selective C-H functionalization of alkenes under environmentally benign conditions represents a useful and attractive yet challenging transformation to access value-added molecules.
Ming-Shang Liu +4 more
doaj +1 more source
Visible Light-Mediated Monofluoromethylation/Acylation of Olefins by Dual Organo-Catalysis
Monofluoromethyl (CH2F) motifs exhibit unique bioactivities and are considered privileged units in drug discovery. The radical monofluoromethylative difunctionalization of alkenes stands out as an appealing approach to access CH2F-containing compounds ...
Jiuli Xia +5 more
doaj +1 more source

