Results 131 to 140 of about 5,480 (194)

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

Angew Chem Int Ed Engl
Escudero J, Long J, Bouëtard D, Morvan J, Koohgard M, Neitzel A, Bockfeld D, Nwachukwu S, Roisnel T, Tykwinski RR, Tamm M, Mauduit M, Trolez Y.   +12 more
europepmc   +1 more source

Covalent Adaptable Networks from Commodity Polybutadiene and Rubber Waste. [PDF]

JACS Au
Hart DR, Georgieva NB, Krajovic DM, Kalow JA.   +3 more
europepmc   +1 more source

Design, Synthesis and ROMP of Novel <i>Exo</i>-Norbornene Silyl Ethers for Functional Polymer Applications. [PDF]

Materials (Basel)
Majchrzak M, Garbarek J, Eissa AM.
europepmc   +1 more source

Polymer Backbone Editing with Cyclopropenes via Olefin Metathesis. [PDF]

ACS Macro Lett
Zhang J, Gutekunst WR.
europepmc   +1 more source

Applications of Olefin Metathesis in the Synthesis of Fluorinated Substrates and Design of Fluorinated Catalysts. [PDF]

Top Curr Chem (Cham)
Semghouli A, Fustero S, Kiss L.
europepmc   +1 more source

2,6-Dioxabicyclo[3.3.1]nonan-3-ones: from natural product treasure troves to synthetic triumphs. [PDF]

RSC Adv
Choudhury UM, Das PP, Mohapatra DK.
europepmc   +1 more source

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Recent Developments in Olefin Cross-Metathesis

Angewandte Chemie - International Edition, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Stephen J Connon, Siegfried Blechert
exaly   +3 more sources

Cross‐Metathesis of Terminal Alkynes

Chemistry – A European Journal, 2014
AbstractTerminal acetylenes are amongst the most problematic substrates for alkyne metathesis because they tend to undergo rapid polymerization on contact with a metal alkylidyne. The molybdenum complex 3 endowed with triphenylsilanolate ligands, however, is capable of inducing surprisingly effective cross‐metathesis reactions of terminal alkyl ...
Lhermet, R., Fürstner, A.
openaire   +3 more sources

Two-directional cross-metathesis

Organic & Biomolecular Chemistry, 2009
Two-directional cross-metathesis of a range of alpha,omega dienes with a variety of electron deficient alkenes has been accomplished. It was found that the process is quite general and gives complete selectivity for the E,E-dienes, making this a very useful and high yielding protocol for two-directional chain elongation.
Annabella F, Newton, Stephen J, Roe, Jean-Christophe, Legeay, Pooja, Aggarwal, Camille, Gignoux, Nicola J, Birch, Robert, Nixon, Marie-Lyne, Alcaraz, Robert A, Stockman   +8 more
openaire   +2 more sources