145491

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Showing 1-9 of 9 results for "145491" within Papers

Polymerization of 1, 3-dienes with iron complexes based catalysts: Influence of the ligand on catalyst activity and stereospecificity.

Ricci G, et al.

J. Mol. Catal. A: Chem., 204, 287-293 (2003)

Cobalt-Catalyzed 1, 4-Hydrobutadienylation of 1-Aryl-1,3-dienes with 2,3-Dimethyl-1,3-butadiene.

Bohn MA, et al.

Angewandte Chemie (International Edition in English), 50(41), 9689-9693 (2011)

Peroxy radical kinetics resulting from the OH-initiated oxidation of 1,3-butadiene, 2,3-dimethyl-1,3-butadiene and isoprene.

Jenkin ME, et al.

Journal of Atmospheric Chemistry, 29(3), 267-298 (1998)

Maleimide scavenging enhances determination of protein S-palmitoylation state in acyl-exchange methods.

Charlotte H Hurst et al.

BioTechniques, 62(2), 69-75 (2017-02-15)

S-palmitoylation (S-acylation) is emerging as an important dynamic post-translational modification of cysteine residues within proteins. Current assays for protein S-palmitoylation involve either in vivo labeling or chemical cleavage of S-palmitoyl groups to reveal a free cysteine sulfhydryl that can be

Thermal [4 + 2] cycloadditions of 3-acetyl-, 3-carbamoyl-, and 3-ethoxycarbonyl-coumarins with 2,3-dimethyl-1,3-butadiene under solventless conditions: a structural study.

Irma Y Flores-Larios et al.

Molecules (Basel, Switzerland), 15(3), 1513-1530 (2010-03-26)

The thermal [4+2] cycloadditions of 3-acetyl-, 3-carbamoyl, and 3-ethoxycarbonylcoumarins with 2,3-dimethyl-1,3-butadiene under solvent free conditions are reported, as well as the epoxidation reactions of some adducts. Discussion is focused on the structural features of the Diels-Alder adducts and their epoxides

Efficient halogen photoelimination from dibromo, dichloro and difluoro tellurophenes.

Carrera EI and Seferos DS.

Dalton Transactions, 44(5), 2092-2096 (2015)

The influence of reaction conditions on the Diels-Alder cycloadditions of 2-thio-3-chloroacrylamides; investigation of thermal, catalytic and microwave conditions.

Marie Kissane et al.

Organic & biomolecular chemistry, 8(24), 5602-5613 (2010-10-12)

The Diels-Alder cycloadditions of cyclopentadiene and 2,3-dimethyl-1,3-butadiene to a range of 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions is described. The influence of reaction conditions on the outcome of the cycloadditions, in particular the stereoselectivity and reaction efficiency, is discussed.

Aryl (hetaryl)-containing gem-cyanonitroethenes: Synthesis, structure, and reactions with 2,3-dimethyl-1,3-butadiene.

Baichurin RI, et al.

Russ. J. Gen. Chem., 85(8), 1845-1854 (2015)

Cycloaddition chemistry of 1, 3-dienes on the silicon (001) surface: Competition between [4+ 2] and [2+ 2] reactions.

Hovis JS, et al.

The Journal of Physical Chemistry B, 102(35), 6873-6879 (1998)

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