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1,1-diarylalkanes (9) 9
chemistry, organic (5) 5
acids (3) 3
alkenes (3) 3
alkylation (2) 2
asymmetric-synthesis (2) 2
chemistry, applied (2) 2
chemistry, multidisciplinary (2) 2
cross-correlations (2) 2
cross-coupling reactions (2) 2
electron ionization (2) 2
electron-rich arenes (2) 2
enantiomers (2) 2
friedel-crafts alkylation (2) 2
rearrangement processes (2) 2
substituent effects (2) 2
1,6-conjugate addition (1) 1
3-hydroxy-3-substituted oxindoles (1) 1
4+1 annulation (1) 1
acylation (1) 1
acylierung (1) 1
alcohols (1) 1
alkyl electrophiles (1) 1
alkyl-halides (1) 1
alkylarylation (1) 1
allylic alcohols (1) 1
aminolysis (1) 1
analysis (1) 1
aromatic compounds (1) 1
aryl (1) 1
asymmetric epoxidation (1) 1
barrier hydrogen-bonds (1) 1
beta-hydride elimination (1) 1
bisphenols (1) 1
c nmr chemical shifts (1) 1
c-13 nmr chemical shifts (1) 1
c-h alkylation (1) 1
c-h bonds (1) 1
calcium (1) 1
carben (1) 1
carbenes (1) 1
carbon double rearrangement (1) 1
carboxylation (1) 1
catalysis (1) 1
catalytic kinetic resolution (1) 1
cations (1) 1
chemistry, physical (1) 1
crafts (1) 1
cyclization (1) 1
desymmetrization (1) 1
diarylation (1) 1
dicarbofunctionalization (1) 1
difunctionalization (1) 1
dihydrocoumarins (1) 1
dynamic kinetic resolution (1) 1
efficient (1) 1
electrophiles (1) 1
enantio-selectivity (1) 1
enantioselective biomimetic cyclization (1) 1
enantioselektivität (1) 1
enzymatic catalysis (1) 1
episulfonium ions (1) 1
ester (1) 1
esters (1) 1
flap inhibitor (1) 1
friedel–crafts alkylation (1) 1
functionalization (1) 1
halides (1) 1
heterocycles (1) 1
heterocyclic-nitrogen-compounds (1) 1
heterocyclische stickstoffverbindungen (1) 1
high-valent nickel (1) 1
homoallylic alcohols (1) 1
hydroarylation (1) 1
hydrocarbons (1) 1
hydrogen (1) 1
hydrogen bonds (1) 1
hydrogen-bond (1) 1
hydrogen-carbon (1) 1
hydrogenation (1) 1
hydroxamic acids (1) 1
hydroxybenzyl alcohols (1) 1
in-situ (1) 1
intermolecular hydroarylation (1) 1
iranium ions (1) 1
mass-spectrometry (1) 1
mathematical models (1) 1
metal-free synthesis (1) 1
methylarylation (1) 1
migratory cross-coupling (1) 1
n-heterocycles (1) 1
n-heterocyclic carbenes (1) 1
n-sulfonyl aldimines (1) 1
natural products (1) 1
negishi arylations (1) 1
nucleophiles (1) 1
nucleophilic carbenes (1) 1
olefins (1) 1
polyene cyclization (1) 1
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Organic Letters, ISSN 1523-7060, 08/2017, Volume 19, Issue 16, pp. 4363 - 4366
The first catalytic, regioselective cross-coupling of 3,4-epoxyalcohol with aryl iodides is reported. The combination of NiCl2·DME and a newly developed C... 
STEREOSPECIFIC FORMATION | HYDROGENATION | HYDROXAMIC ACIDS | ALLYLIC ALCOHOLS | RETENTION | HOMOALLYLIC ALCOHOLS | TOLTERODINE | ASYMMETRIC EPOXIDATION | CHEMISTRY, ORGANIC | 1,1-DIARYLALKANES | AMINOLYSIS
Journal Article
ACS Catalysis, ISSN 2155-5435, 01/2018, Volume 8, Issue 1, pp. 310 - 313
1,1-Diarylalkanes are important structural frameworks which are widespread in biologically active molecules. Herein, we report a reductive relay cross-coupling... 
alkyl electrophiles | high-valent nickel | 1,1-diarylalkanes | migratory cross-coupling | β-hydride elimination | HALIDES | HYDROCARBONS | NEGISHI ARYLATIONS | UNACTIVATED TERTIARY ALKYL | SECONDARY | CHEMISTRY, PHYSICAL | FUNCTIONALIZATION | beta-hydride elimination | STEREOCENTERS | CARBOXYLATION | REMOTE | ELECTROPHILES
Journal Article
ORGANIC PROCESS RESEARCH & DEVELOPMENT, ISSN 1083-6160, 08/2019, Volume 23, Issue 8, pp. 1686 - 1694
We report a five-step synthesis of the biologically important 1,1-diarylalkane 1, a potential 5-lipoxygenase activating protein (FLAP) inhibitor that was... 
ACIDS | CHEMISTRY, ORGANIC | three-component | REDUCTIVE DICARBOFUNCTIONALIZATION | UNACTIVATED OLEFINS | alkenes | ZINC | ALKYL-HALIDES | DIFUNCTIONALIZATION | 1,1-diarylalkanes | CROSS-COUPLING REACTIONS | FLAP inhibitor | dicarbofunctionalization | ARYL | CHEMISTRY, APPLIED | alkylarylation | TERMINAL ALKENES | CYCLIZATION
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2017, Volume 23, Issue 10, pp. 2275 - 2281
Journal Article
Chinese Journal of Organic Chemistry, ISSN 0253-2786, 05/2017, Volume 37, Issue 5, pp. 1160 - 1164
A novel iron catalyzed hydroarylation, methylarylation, and diarylation of styrenes to form unsymmetrical 1,1-diarylalkanes with electron rich anisole and... 
Hydroarylation | Vinylarenes | Diarylation | 1,1-diarylalkanes | Methylarylation | ROOM-TEMPERATURE | STYRENES | CHEMISTRY, ORGANIC | vinylarenes | UNACTIVATED ARENES | ALKENES | CALCIUM | OLEFINS | hydroarylation | methylarylation | INTERMOLECULAR HYDROARYLATION | FRIEDEL-CRAFTS ALKYLATION | ELECTRON-RICH ARENES | EFFICIENT | diarylation
Journal Article
by Cheng, YY and Fang, ZQ and Jia, YW and Lu, ZY and Li, WJ and Li, PF
RSC ADVANCES, 08/2019, Volume 9, Issue 42, pp. 24212 - 24217
The enantioselective conjugate addition of 2-naphthols to ortho-hydroxyphenyl substituted para-quinone methides has been achieved with the aid of a chiral... 
C(SP)-H BONDS | 1,6-CONJUGATE ADDITION | ASYMMETRIC-SYNTHESIS | ACIDS | ALKYLATION | HYDROXYBENZYL ALCOHOLS | 1,1-DIARYLALKANES | 4+1 ANNULATION | CHEMISTRY, MULTIDISCIPLINARY | IN-SITU | DIHYDROCOUMARINS
Journal Article
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