Results 81 to 90 of about 4,618,245 (281)

Synthesis of Conjugated Linear and Cyclic Polyynes by Selective Alkyne Metathesis. [PDF]

open access: yesAngew Chem Int Ed Engl
The formation of polyynes with an odd number of conjugated triple bonds is challenging, particularly for complex architectures since most established methods rely on irreversible C–C bond‐forming reactions. To address this, we have developed the synthesis of triynes via alkyne metathesis.
Escudero J   +12 more
europepmc   +3 more sources

Alkene Chemoselectivity in Ruthenium-Catalyzed Z-Selective Olefin Metathesis [PDF]

open access: yes, 2013
Chelated ruthenium catalysts can facilitate highly chemoselective olefin metathesis. Terminal and internal Z olefins reacted selectively to form new Z olefins in the presence of internal E olefins.
Cannon, Jeffrey S., Grubbs, Robert H.
core   +2 more sources

“Zipped Synthesis” by Cross-Metathesis Provides a Cystathionine β-Synthase Inhibitor that Attenuates Cellular H2S Levels and Reduces Neuronal Infarction in a Rat Ischemic Stroke Model

open access: yesACS Central Science, 2016
The gaseous neuromodulator H2S is associated with neuronal cell death pursuant to cerebral ischemia. As cystathionine β-synthase (CBS) is the primary mediator of H2S biogenesis in the brain, it has emerged as a potential target for the treatment of ...
Christopher D. McCune   +9 more
semanticscholar   +1 more source

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

Synthetic Approaches to Diospongins: A Two Decade Journey

open access: yesSynOpen, 2022
Tetrahydropyran units having multiple stereogenic centers serve as excellent building blocks for various active pharmaceutical ingredients (APIs). In particular, the presence of the unique molecular architecture of the trisubstituted tetrahydropyran (THP)
Krishnaji Tadiparthi, Sourav Chatterjee
doaj   +1 more source

Substituted Pyrroles via Olefin Cross-Metathesis

open access: yesOrganic Letters, 2010
Olefin cross-metathesis (CM) provides a short and convenient entry to diverse trans-γ-aminoenones. When exposed to either acid or Heck arylation conditions, these intermediates are converted to mono-, di-, or trisubstituted pyrroles. The value of this chemistry is demonstrated by its application to the tetrasubstituted pyrrole subunit of Atorvastatin.
Donohoe, TJ   +3 more
openaire   +3 more sources

New library of aminosulfonyl-tagged Hoveyda–Grubbs type complexes: Synthesis, kinetic studies and activity in olefin metathesis transformations

open access: yesBeilstein Journal of Organic Chemistry, 2010
Seven novel Hoveyda–Grubbs precatalysts bearing an aminosulfonyl function are reported. Kinetic studies indicate an activity enhancement compared to Hoveyda’s precatalyst.
Etienne Borré   +3 more
doaj   +1 more source

A Short and Efficient Total Synthesis of Ficuseptamines A and B

open access: yesMolecules, 2018
A rapid and efficient total synthesis of ficuseptamines A and B by a cross metathesis strategy is described.
Hani Mutlak A. Hassan
doaj   +1 more source

Olefin metathesis transformations in thermomorphic multicomponent solvent systems [PDF]

open access: yes, 2015
International ...
Bilel, Hallouma   +5 more
core   +3 more sources

Synthesis and Evaluation of Molybdenum and Tungsten Monoaryloxide Halide Alkylidene Complexes for Z-Selective Cross-Metathesis of Cyclooctene and Z-1,2-Dichloroethylene.

open access: yesJournal of the American Chemical Society, 2016
Molybdenum complexes with the general formula Mo(NR)(CHR')(OR″)(Cl)(MeCN) (R = t-Bu or 1-adamantyl; OR″ = a 2,6-terphenoxide) recently have been found to be highly active catalysts for cross-metathesis reactions between Z-internal olefins and Z-1,2 ...
J. K. Lam   +5 more
semanticscholar   +1 more source

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