Results 31 to 40 of about 18,717 (339)

Reductive Arylation of Arylidene Malonates Using Photoredox Catalysis.

open access: yesACS Catalysis, 2019
A strategy with arylidene malonates provides access to β-umpolung single-electron species. Reported here is the utilization of these operators in intermolecular radical-radical arylations, while avoiding conjugate addition/dimerization reactivity that is
Rick C. Betori, K. Scheidt
semanticscholar   +1 more source

CHROM-MALONATES. [PDF]

open access: yesJournal of the American Chemical Society, 1903
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openaire   +1 more source

Lewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic esters [PDF]

open access: yes, 2009
Herein we report that simple Lewis acids catalyze the hydroarylation of benzylidene malonates with phenols. Ultimately, 3,4-disubstituted dihydrocoumarins are obtained via a hydroarylation-lactonization sequence. Moreover, the dihydrocoumarins are formed
Duan, Shaofeng   +2 more
core   +1 more source

Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water [PDF]

open access: yes, 2014
Tenbrink K, Kemker I, Schatz J, Gröger H. Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water. ARKIVOC. 2015;2015(2):10-19.A range of substituted cycloalkene-1,1-dicarboxylates was synthesized through olefin metathesis ...
Gröger, Harald   +3 more
core   +2 more sources

Pd‐Catalyzed C−C, C−N, and C−O Bond‐Forming Difunctionalization Reactions of Alkenes Bearing Tethered Aryl/Alkenyl Triflates [PDF]

open access: yes, 2020
Over the past few years our group has described a new type of alkene difunctionalization reaction in which aryl or alkenyl triflates bearing tethered alkenes are coupled with various nucleophiles to afford carbocyclic products. The products are formed in
Bornowski, Evan C.   +2 more
core   +1 more source

Supramolecular Gels as Active Tools for Reaction Engineering

open access: yesAngewandte Chemie, EarlyView.
The unique combination of environments within gels, self‐assembled from low‐molecular‐weight gelators, offers the ability to control reactivity in new ways, achieving unique reaction outcomes, leading to the emerging concept of supramolecular gels as nanoreactors. Smart chemical engineering methods enable the use of such gels to fabricate materials and
David K. Smith
wiley   +2 more sources

Synthesis of New C2- Symmetric Fluoren-9-ylidene Malonate Derived Bis(oxazoline) Ligands and Their Application in Friedel-Crafts Reactions

open access: yesMolecules, 2010
A series of new C2-symmetric fluoren-9-ylidene malonate-derived bis(oxazoline) ligands were synthesized from fluoren-9-ylidene malonate and enantiomerically pure amino alcohols via a convenient route.
Lei Liu   +3 more
doaj   +1 more source

Intermolecular Reductive Couplings of Arylidene Malonates via Lewis Acid/Photoredox Cooperative Catalysis.

open access: yesOrganic Letters, 2018
A cooperative Lewis acid/photocatalytic reduction of arylidene malonates yields a versatile radical anion species. This intermediate preferentially undergoes intermolecular radical-radical coupling reactions, and not the conjugate addition-dimerization ...
Benjamin R. McDonald, K. Scheidt
semanticscholar   +1 more source

The Potential of an Itaconic Acid Diester as Environmentally Friendly Plasticizer for Injection‐Molded Polylactide Parts

open access: yesMacromolecular Materials and Engineering, Volume 307, Issue 12, December 2022., 2022
Dibutyl itaconate (DBI) is tested as an environmentally friendly plasticizer for polylactide (PLA) with different proportions of DBI in the 2.5‐20 wt.% range. A co‐rotating twin‐screw extrusion process and injection moulding is employed for the manufacturing of the samples. As a result, noticeable increase in the elongation at break from 4.6% (neat PLA)
Juan Ivorra‐Martinez   +4 more
wiley   +1 more source

Benzamide‐Directed Hydroarylative Cross‐Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters

open access: yesAngewandte Chemie, EarlyView.
Benzamide‐directed iridium‐catalyzed branched selective and enantioselective C(sp2)‐H additions to minimally activated alkenes give tertiary and quaternary benzylic stereocenters under byproduct‐free conditions. The processes are enabled by a family of SPINOL‐based homochiral diphosphonite ligands.
Timothy P. Aldhous   +9 more
wiley   +2 more sources

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