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Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 40, pp. 12343 - 12346
Use of a tandem ring‐opening–ring‐closing metathesis (RORCM) strategy for the synthesis of functional metathesis catalysts is reported. Ring opening of 7... 
olefin metathesis | heterotelechelic polymers | polymerization | ruthenium | Grubbs catalysts | Catalysts | Polymerization | Thermodynamics | Ruthenium | Functional anatomy | Metathesis | Decomposition reactions | Forming | Chemical synthesis | Bonding | Ring opening
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2015, Volume 54, Issue 17, pp. 5018 - 5024
Olefin cross metathesis is a particularly powerful transformation that has been exploited extensively for the formation of complex products... 
olefin metathesis | natural products | Z‐alkenes | cross metathesis | Z-alkenes | Cross metathesis | Olefin metathesis | Natural products | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Ruthenium | Catalysts | Olefins | Decomposition reactions | Metathesis | Alkylidene | Formations | Terminals | Catalysis
Journal Article
Catalysis letters, ISSN 1011-372X, 3/2014, Volume 144, Issue 3, pp. 373 - 379
Nine biotinylated Grubbs–Hoveyda and Grubbs-type metathesis catalysts were synthesized and evaluated in ring closing metathesis reactions of N-tosyl diallylamine and 5-hydroxy-2-vinylphenyl acrylate... 
Aqueous catalysis | Ring closing metathesis | Chemistry | Physical Chemistry | Organometallic Chemistry | Fluorescence assay | Hoveyda–Grubbs | Catalysis | Industrial Chemistry/Chemical Engineering | Coumarin | Hoveyda-Grubbs | Biotin | Ruthenium | Chemical properties | Catalysts | Olefins | Metathesis | Catalytic activity | Chemical synthesis
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 07/2007, Volume 129, Issue 26, pp. 8207 - 8216
... = methyl or phenyl, X = CH2CH3, OCH3, or OSiH3, and Y = CH2CH3, OCH3, or OSiH3, which are representative of experimental olefin metathesis catalysts, and the results are compared to those previously obtained for Re(⋮CCH3)(CHCH3)(X)(Y... 
or physical chemistry | Chemical Sciences | Theoretical and
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2017, Volume 56, Issue 37, pp. 11213 - 11216
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 06/2007, Volume 129, Issue 25, pp. 7961 - 7968
Journal Article
Nature (London), ISSN 1476-4687, 04/2016, Volume 533, Issue 7603, pp. 374 - 379
The olefin metathesis reaction of two unsaturated substrates is one of the most powerful carbon-carbon-bond-forming reactions in organic chemistry... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Carbonyl compounds | Olefins | Chemical research | Chemical reactions | Iron | Chemical properties | Research | Organic chemistry | Acids | Chemical bonds | Polymerization | Titanium | Carbon
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2015, Volume 54, Issue 42, pp. 12384 - 12388
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2015, Volume 54, Issue 1, pp. 215 - 220
Molybdenum‐, tungsten‐, and ruthenium‐based complexes that control the stereochemical outcome of olefin metathesis reactions have been recently introduced... 
enantioselective synthesis | olefin metathesis | neopeltolide | catalysis | leucascandrolide A | Catalysis | Leucascandrolide a | Neopeltolide | Olefin metathesis | Enantioselective synthesis | Synthesis | Ruthenium | Enantiomers | Olefins | Organic compounds | Index Medicus | Design engineering | Catalysts | Decomposition reactions | Metathesis | Strategy | Transformations
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 09/2018, Volume 24, Issue 54, pp. 14295 - 14301
...‐heterocyclic carbene (NHC) catalysts for olefin metathesis. Starting from Mo(NR)(CHCMe2R′)(OTf)2⋅DME (R=alkyl, aryl; R′=CH3, Ph; OTf=CF3SO3; DME=1,2‐dimethoxyethane), W(NR... 
tungsten | metathesis | alkylidenes | molybdenum | N-heterocyclic carbenes | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Catalysts | Heterocyclic compounds | Molybdenum | Olefins | Tungsten | Alkoxides | Metathesis | Decomposition reactions | Polymerization | Substitution reactions | Immobilization | Sulfonates | Carboxylic acids | Alcohols | Stereoselectivity | Aromatic compounds | Betaine | Alkylidene | Ligands | Catalysis | Functional groups
Journal Article
Macromolecules, ISSN 0024-9297, 06/2018, Volume 51, Issue 12, pp. 4564 - 4571
Ru-based metathesis catalysts employed in cyclopolymerization (CP) of 1,6-heptadiyne derivatives have promoted regioselective α... 
Polymer Science | Physical Sciences | Science & Technology
Journal Article