Results 91 to 100 of about 17,341 (257)
With the help of the smaller brother: Although alkyne metathesis will always be the little brother of alkene metathesis, it allows problems to be solved that are currently beyond reach of the more famous sibling.
Fürstner, A. +4 more
core +1 more source
A New Ruthenium-Based Olefin Metathesis Catalyst Coordinated with 1,3-Dimesityl-1,4,5,6-tetrahydropyrimidin-2-ylidene: Synthesis, X-ray Structure, and Reactivity [PDF]
The new ruthenium olefin metathesis catalyst 4 bearing a 5,5‘-dimethyl-1,3-dimesityl-1,4,5,6-tetrahydropyrimidin-2-ylidene ligand was first synthesized from (PCy_3)_2(Cl)_2Ru ═ CHPh (1).
Grubbs, Robert H. +2 more
core +1 more source
Nonproductive Events in Ring-Closing Metathesis Using Ruthenium Catalysts [PDF]
The relative TONs of productive and nonproductive metathesis reactions of diethyl diallylmalonate are compared for eight different ruthenium-based catalysts. Nonproductive cross metathesis is proposed to involve a chain-carrying ruthenium methylidene.
Grubbs, Robert H. +4 more
core +2 more sources
We have developed a simple methodology to transform cis-syn-cis-triquinane derivative 2 into the diindole based macrocycle 6 involving Fischer indolization and ring-closing metathesis (RCM).
Sambasivarao Kotha +2 more
doaj +1 more source
Synthesis, Structure, and Activity of Enhanced Initiators for Olefin Metathesis [PDF]
A series of ruthenium olefin metathesis catalysts of the general structure (H_2IMes)(PR_3)(Cl)_2Ru CHPh (H_2IMes = 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene) have been prepared; these complexes are readily accessible in two steps from commercially ...
Day, Michael W. +3 more
core +1 more source
Toward a simulation approach for alkene ring-closing metathesis : scope and limitations of a model for RCM [PDF]
A published model for revealing solvent effects on the ring-closing metathesis (RCM) reaction of di-Et diallylmalonate 7 has been evaluated over a wider range of conditions, to assess its suitability for new applications.
Adjiman C. S. +33 more
core +1 more source
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley +1 more source
Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding
Andrzej Tracz +3 more
doaj +1 more source
Rapid assembly of highly-functionalised difluorinated cyclooctenones via ring-closing metathesis [PDF]
Building block methodology from trifluoroethanol and ringclosing metathesis using a Fürstner modification of Grubbs’ conditions allows the rapid synthesis of novel difluorinated ...
Kariuki, Benson M. +7 more
core +1 more source
Distinct Ligand‐ and Metal‐Centered Phosphorescence in a Terbium Carbazolyl Complex
Terbium and lanthanum carbazolide complexes show two distinct modes of luminescence: Strongly temperature‐dependent narrow‐line terbium emission could be induced. In addition, both the terbium and the lanthanum complexes show broad‐line interligand emission processes with excited states of microsecond life‐time.
Xiaofei Sun +9 more
wiley +1 more source

