X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
to-tail dimerization (120) 120
chemistry, multidisciplinary (55) 55
chemistry, organic (55) 55
catalysis (31) 31
dimerization (31) 31
chemistry, inorganic & nuclear (30) 30
umpolung (28) 28
complexes (27) 27
carbenes (26) 26
methyl acrylate (24) 24
mechanism (21) 21
carben (17) 17
polymerization (16) 16
reactivity (16) 16
ruthenium (16) 16
activation (15) 15
chemistry, physical (15) 15
index medicus (15) 15
n-heterocyclic carbene (15) 15
derivatives (13) 13
ligand (13) 13
palladium (13) 13
alkynes (12) 12
n-heterocyclic carbenes (12) 12
selective dimerization (12) 12
baylis-hillman reaction (11) 11
catalysts (11) 11
conjugate-addition (11) 11
methyl-methacrylate (11) 11
organocatalysis (11) 11
polymer science (11) 11
stereoselective dimerization (11) 11
stereoselective-synthesis (11) 11
acrylates (10) 10
enynes (10) 10
heterocyclic compounds (10) 10
ring-opening polymerization (10) 10
terminal alkynes (10) 10
aldehydes (9) 9
chemical properties (9) 9
dimerisation (9) 9
rh catalysts (9) 9
stable carbene (9) 9
chemistry (8) 8
head-to-tail (8) 8
head-to-tail dimerization (8) 8
oligomerization (8) 8
reaction-mechanism (8) 8
reaktionsmechanismus (8) 8
bond-forming reactions (7) 7
chemical reactions (7) 7
crystal-structure (7) 7
crystal-structures (7) 7
frustrated lewis pairs (7) 7
ligands (7) 7
monomers (7) 7
olefins (7) 7
organic chemistry (7) 7
proton-transfer polymerization (7) 7
titanium (7) 7
acetylenes (6) 6
alkine (6) 6
biochemistry & molecular biology (6) 6
catalyzed reactions (6) 6
cyclization (6) 6
density functionals (6) 6
esters (6) 6
substrates (6) 6
acrylate (5) 5
acrylonitrile (5) 5
alkenes (5) 5
alkyne dimerization (5) 5
alpha,beta-unsaturated aldehydes (5) 5
alpha-olefins (5) 5
carbon (5) 5
chemical synthesis (5) 5
cross-dimerization (5) 5
diels-alder reactions (5) 5
domino reactions (5) 5
enantioselective synthesis (5) 5
gamma-butyrolactones (5) 5
highly efficient (5) 5
molecular-structure (5) 5
monomer (5) 5
nhc catalysis (5) 5
nucleophilic carbenes (5) 5
permethyltitanocene (5) 5
polymerisation (5) 5
polymers (5) 5
rauhut-currier reaction (5) 5
reaction mechanisms (5) 5
reduction (5) 5
regioselective dimerization (5) 5
research (5) 5
stereoselectivity (5) 5
stetter reaction (5) 5
titanocene (5) 5
transition-metal-complexes (5) 5
tweezer complexes (5) 5
acid (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Angewandte Chemie International Edition, ISSN 1433-7851, 05/2017, Volume 56, Issue 22, pp. 6317 - 6320
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 06/2014, Volume 9, Issue 6, pp. 1530 - 1534
The construction of supramolecular systems in aqueous media is still a great challenge owing to the limited sources of building blocks. In this study, a series... 
dimerization | cucurbituril | host–guest systems | head‐to‐tail | self‐assembly | self-assembly | head-to-tail | host-guest systems | POLYMERS | COMPLEXES | HOST | CHEMISTRY, MULTIDISCIPLINARY | NANOPARTICLES | PI INTERACTION | SOLUBLE SUPRAMOLECULAR POLYMERIZATION | CHEMISTRY | CHARGE-TRANSFER INTERACTIONS | ASSOCIATION | SELECTIVITY
Journal Article
Synthesis, ISSN 0039-7881, 08/2013, Volume 45, Issue 15, pp. 2088 - 2092
Journal Article
Physical Chemistry Chemical Physics, ISSN 1463-9076, 08/2014, Volume 16, Issue 37, pp. 20001 - 20008
Reaction mechanisms of the N-heterocyclic carbene (NHC)-catalyzed dimerization of methyl methacrylate were studied using density functional theory (DFT... 
DENSITY FUNCTIONALS | PATH | KETENES | DIELS-ALDER REACTIONS | TO-TAIL DIMERIZATION | ENANTIOSELECTIVE SYNTHESIS | 4+2 CYCLOADDITION | SELECTIVE DIMERIZATION | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | RUTHENIUM | ACRYLATE
Journal Article
Physical Chemistry Chemical Physics, ISSN 1463-9076, 08/2014, Volume 16, Issue 37, pp. 20001 - 20008
Reaction mechanisms of the N-heterocyclic carbene (NHC)-catalyzed dimerization of methyl methacrylate were studied using density functional theory (DFT... 
Catalysts | Mathematical analysis | Polymethyl methacrylates | Catalysis | Reaction mechanisms | Carbenes | Dimerization | Channels
Journal Article
Synthesis, ISSN 0039-7881, 09/2017, Volume 49, Issue 17, pp. 3962 - 3967
Abstract A neutral metal-free system for the head-to-tail dimerization of electron-rich alkenes with stoichiometric amount of BrCCl 2 H and NaI is reported... 
paper | dimerization | BrCCl | head-to-tail | electron-rich alkenes | metal-free | BrCCl2H | STYRENES | VINYLARENES | CHEMISTRY, ORGANIC | CATALYST | EFFICIENT
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 05/2016, Volume 314, pp. 182 - 200
•The homo- and cross-dimerizations by transition-metal compounds are reviewed.•The first solid evidence for the tail-to-tail dimerizations of substituted alkenes by the oxidative coupling mechanism is described... 
Ruthenium catalyst | Substituted alkene | Enantioselective cross-dimerization | Oxidative coupling mechanism | Dimerization | TO-TAIL DIMERIZATION | SELECTIVE DIMERIZATION | CRYSTAL-STRUCTURE | CONJUGATED DIENES | STRUCTURAL-CHARACTERIZATION | METHYL ACRYLATE | INTRAMOLECULAR CYCLOADDITION | CHEMISTRY, INORGANIC & NUCLEAR | H BOND ACTIVATION | PI-ALLYLIC COMPLEXES | HOMOGENEOUS CATALYSIS
Journal Article
ACS Catalysis, ISSN 2155-5435, 09/2015, Volume 5, Issue 9, pp. 5328 - 5332
A room-temperature dimerization of crotonates into 2-ethylidene-3-methylpentanedioates provides a sustainable route to difunctional monomers for step-growth polymerizations... 
dimerization | base catalysis | alkenoates | monomer synthesis | N-heterocyclic carbenes | ACID | TO-TAIL DIMERIZATION | CHEMISTRY, PHYSICAL | GROUP-TRANSFER POLYMERIZATION | NITRILES | CARBONYL | POLYHYDROXYALKANOATES | ALPHA,BETA-UNSATURATED ESTERS | UMPOLUNG | ACRYLATES
Journal Article
Organic Letters, ISSN 1523-7060, 02/2014, Volume 16, Issue 3, pp. 948 - 951
A counterion-controlled reactivity tuning in Pd-catalyzed highly chemoselective and regioselective dimerization and hydration of terminal alkynes is reported... 
PALLADIUM | REGIOSELECTIVE HYDRATION | ACID-CATALYZED HYDRATION | TO-TAIL DIMERIZATION | ARYLACETYLENES | COMPLEXES | CHEMISTRY, ORGANIC | OLIGOMERIZATION | CYCLIZATION | SOLVENT | ENYNES
Journal Article
Catalysis Communications, ISSN 1566-7367, 02/2017, Volume 90, pp. 95 - 99
...-to-tail dimerization of vinylarenes over heterogeneous catalyst (Snβ zeolite). The scope of the reaction was explored for various 1-arylethanols and afforded... 
Alkenes | Heterogeneous catalysts | Dimerization | Zeolites | Alcohols | CATALYZED DIMERIZATION | TO-TAIL DIMERIZATION | LEWIS-ACID | ACYLATION | SELECTIVE DIMERIZATION | LIQUID | CHEMISTRY, PHYSICAL | MOLECULAR-SIEVES | SOLID ACIDS | ACETIC-ACID | TIN-SILICATE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2018, Volume 57, Issue 37, pp. 12003 - 12006
The mechanism and selectivity of terminal alkyne coupling reactions promoted by rhodium(I) complexes of NHC‐based CNC pincer ligands have been investigated.... 
pincer ligands | C−C coupling | macrocyclic ligands | enynes | rhodium | C-C coupling | TO-TAIL DIMERIZATION | COMPLEXES | CROSS-DIMERIZATION | CHEMISTRY, MULTIDISCIPLINARY | Rhodium | Ligands | Chemical reactions | Selectivity | Topology | Coupling | Computer numerical control | Alkynes | Communications | Communication
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2009, Volume 351, Issue 9, pp. 1371 - 1377
Dimerization of N‐protected propargylic amines in a rather rare head‐to‐tail mode has been achieved under mild conditions with high selectivity using rhodium catalysts. The N... 
gold | head‐to‐tail dimerization | enynes | propargylic amines | hydroamination | RECOGNITION | SUBSTITUTED PYRROLES | COMPLEXES | INTRAMOLECULAR HYDROAMINATION | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | CROSS-DIMERIZATION | head-to-tail dimerization | STEREOSELECTIVE DIMERIZATION | CYCLOISOMERIZATION | HIGHLY EFFICIENT SYNTHESIS | LIGAND | CHEMISTRY, APPLIED
Journal Article
ACS catalysis, ISSN 2155-5435, 02/2019, Volume 9, Issue 2, pp. 810 - 818
... = N-heterocyclic carbene) toward the gem-specific dimerization of terminal alkynes. In comparison to our first-generation catalyst, the newly synthesized catalyst is more active and features the same geminal specificity... 
N-heterocyclic carbene | catalysis | iron | alkyne dimerization | enyne | computation | PALLADIUM | TO-TAIL DIMERIZATION | ATOM ECONOMY | COMPLEXES | REGIOSELECTIVE DIMERIZATION | CHEMISTRY, PHYSICAL | INTERNAL ALKYNES | STEREOSELECTIVE DIMERIZATION | SELECTIVE CROSS-DIMERIZATION | LIGAND
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2014, Volume 356, Issue 16, pp. 3314 - 3318
Journal Article