Results 31 to 40 of about 17,341 (257)

Light-induced olefin metathesis

open access: yesBeilstein Journal of Organic Chemistry, 2010
Light activation is a most desirable property for catalysis control. Among the many catalytic processes that may be activated by light, olefin metathesis stands out as both academically motivating and practically useful.
Yuval Vidavsky, N. Gabriel Lemcoff
doaj   +1 more source

Ring closing metathesis in protic media by means of a neutral and polar ruthenium benzylidene complex [PDF]

open access: yes, 2002
The ring closing olefine metathesis in protic solvents using a new ruthenium benzylidene complex is ...
Grubbs, Robert H., Rölle, Thomas
core   +1 more source

Ring Rearrangement Metathesis in 7-Oxabicyclo[2.2.1]heptene (7-Oxanorbornene) Derivatives. Some Applications in Natural Product Chemistry

open access: yesNatural Product Communications, 2017
Metathesis reactions is firmly established as a valuable synthetic tool in organic chemistry, clearly comparable with the venerable Diels-Alder and Wittig reactions and, more recently, with the metal-catalyzed cross-coupling reactions.
Silvia Roscales, Joaquín Plumet
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.
Kilbinger, Andreas F. M.   +3 more
core   +1 more source

One-pot synthesis of 5-amino-2,5-dihydro-1-benzoxepines: access to pharmacologically active heterocyclic scaffolds [PDF]

open access: yes, 2015
A one-pot multibond-forming process involving a thermally mediated Overman rearrangement and a ring closing metathesis reaction of allylic trichloroacetimidates bearing a 2-allyloxyaryl group has been developed for the synthesis of 5-amino-substituted 2 ...
Calder, Ewen D.D.   +3 more
core   +2 more sources

Merging Biocatalysis and Chemocatalysis in Flow: State‐of‐the‐Art and Future Directions for Sustainable Synthesis

open access: yesAngewandte Chemie, EarlyView.
This review highlights recent advances in integrating biocatalysis and chemocatalysis in continuous flow to create streamlined, sustainable processes. It examines chemo‐enzymatic cascades combining at least one enzymatic and one chemical step, discusses challenges such as enzyme immobilization, leaching, and reactor clogging, and presents solutions ...
Petros Siasiaridis   +2 more
wiley   +2 more sources

Olefin metathesis in nano-sized systems

open access: yesBeilstein Journal of Organic Chemistry, 2011
The interplay between olefin metathesis and dendrimers and other nano systems is addressed in this mini review mostly based on the authors’ own contributions over the last decade.
Didier Astruc   +7 more
doaj   +1 more source

Synthesis of Highly Stable 1,3-Diaryl-1H-1,2,3-triazol-5-ylidenes and Their Applications in Ruthenium-Catalyzed Olefin Metathesis [PDF]

open access: yes, 2011
The formal cycloaddition between 1,3-diaza-2-azoniaallene salts and alkynes or alkyne equivalents provides an efficient synthesis of 1,3-diaryl-1H-1,2,3-triazolium salts, the direct precursors of 1,2,3-triazol-5-ylidenes.
Bertrand, Guy   +6 more
core   +2 more sources

The Far Side of Carboranes: Anticancer Active Monocations and Ambiently Stable Dications

open access: yesAngewandte Chemie, EarlyView.
This work describes the synthesis of bench‐stable dicationic carboranes. Their enhanced electrophilicity is documented by opening the clusters with weak nucleophiles or dihydrogen. The surprising stability of positively charged carboranes in water enabled a study of their in vitro antiproliferative activity, which surpassed the effects of doxorubicin ...
Vlastimil Němec   +10 more
wiley   +2 more sources

Stereoselectivity of Macrocyclic Ring-Closing Olefin Metathesis [PDF]

open access: yesOrganic Letters, 2000
[reaction: see text] Macrocyclic ring-closing olefin metathesis using ruthenium catalyst 3 was performed to produce a 14-membered lactone. The E/Z ratio of lactone was high regardless of the R group (auxiliary) or the initial alkene stereochemistry.
Lee, Choon Woo, Grubbs, Robert H.
openaire   +4 more sources

Home - About - Disclaimer - Privacy