Results 61 to 70 of about 9,389 (255)

Solution Synthesis of Actinide Chalcogenide and Oxychalcogenide Nanoparticles

open access: yesAngewandte Chemie, EarlyView.
We report the synthesis of UOS, UOSe, and US2 nanoparticles under colloidal conditions. The magnetic properties were measured of all three materials and compared to prior studies of UO2 nanoparticles. Nanoparticle phases were determined using powder diffraction, and size by transmission electron microscopy.
Cheyenne Orozco   +7 more
wiley   +2 more sources

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

open access: yesSynOpen, 2023
This review reports the synthesis of various bioactive macrocycles, involving ring-closing metathesis as a key step, developed since ca. 2000. These macrocycles exhibited biological activities such as antiviral, antifungal, antibacterial, and anticancer ...
Nasrin Jahan, Inul Ansary
doaj   +1 more source

Ring Closing Metathesis Reaction

open access: yes, 1999
Various spiro cyclic systems are prepared from β-di-carbonyl compounds and active methylene substrates via palladium catalyzed allylation and ring-closing metathesis (RCM) reaction as key ...
Ashoke Deb   +9 more
core   +1 more source

Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics

open access: yesBeilstein Journal of Organic Chemistry, 2015
Alkenes containing N-heteroaromatics are known to be poor partners in cross-metathesis reactions, probably due to catalyst deactivation caused by the presence of a nitrogen atom.
Kevin Lafaye   +4 more
doaj   +1 more source

Total Synthesis of (-)-(7S,10R)-Calamenene and (-)-(7S,10R)-2-Hydroxycalamenene by Use of a Ring-Closing Metathesis Reaction. A Comparison of the cis- and trans-Isomers

open access: yesMolecules, 2002
The title compounds have been synthesized starting from l-menthone by application of a ring-closing metathesis reaction to confirm their reported absolute and relative stereochemistry.
Yoshinori Asakawa   +5 more
doaj   +1 more source

Functional Metathesis Catalyst Through Ring Closing Enyne Metathesis: One Pot Protocol for Living Heterotelechelic Polymers [PDF]

open access: yes, 2018
Enyne ring closing metathesis has been used to synthesize functional group carrying metathesis catalysts from a commercial (Ru-benzylidene) Grubbs’ catalysts.
Lucarini, Fiorella   +12 more
core   +1 more source

1,7‐Digallatetracarborane: Between Nucleophilic closo‐Cluster and “Inverse Sandwich” Digallylene

open access: yesAngewandte Chemie, EarlyView.
A dianionic π‐ligand is used to make a Janus‐type twofold complex with low‐valent gallium Ga(+I). The resulting compound can be seen as and reveals the reactivity of both: a Wade‐type closo‐carborane cluster with nucleophilic Ga‐sites, as well as π‐ligand stabilized Ga(I) atoms in an inverse sandwich compound.
Julijan Sarcevic   +4 more
wiley   +2 more sources

A Synthetic Approach Toward a Brominated Oxocane Labdane Diterpenoid Isolated From

open access: yesNatural Product Communications, 2020
The synthesis of a labdane oxocane epoxy-alcohol is described starting from the Wieland–Miescher ketone derivative via ring closing olefin metathesis of a diene derivative, targeting the total synthesis of a brominated oxocane labdane diterpenoid ...
Hisahiro Hagiwara   +4 more
doaj   +1 more source

Heavier Alkyne‐Ni0 Complexes, [R2E2·Ni] (E = Sn, Pb), Exhibiting σ‐Complex Character

open access: yesAngewandte Chemie, EarlyView.
Using a reductive group elimination strategy, heavier alkyne (LEEL; E = Sn, Pb) complexes of Ni0 are accessed. In contrast to classical alkyne coordination, these systems are best described as σ‐complexes, driven by ligand‐induced constraints and the established poor π‐bonding in heavier alkyne analogues.
Leopold Junge   +3 more
wiley   +2 more sources

Efficient catalytic alkyne metathesis with a fluoroalkoxy-supported ditungsten(III) complex

open access: yesBeilstein Journal of Organic Chemistry, 2018
The molybdenum and tungsten complexes M2(OR)6 (Mo2F6, M = Mo, R = C(CF3)2Me; W2F3, M = W, R = OC(CF3)Me2) were synthesized as bimetallic congeners of the highly active alkyne metathesis catalysts [MesC≡M{OC(CF3)nMe3−n}] (MoF6, M = Mo, n = 2; WF3, M = W ...
Henrike Ehrhorn   +3 more
doaj   +1 more source

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