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2,2'-bisbiphenyl (4) 4
chemistry, organic (4) 4
2,2′-bisbiphenyl (2) 2
analogs (2) 2
assignment of absolute configuration (2) 2
asymmetric heck reaction (2) 2
chemistry, inorganic & nuclear (2) 2
chemistry, multidisciplinary (2) 2
enantioselective hydrogenation (2) 2
ene reactions (2) 2
hetero-diels-alder (2) 2
meo-biphep derivatives (2) 2
2,2 '-bis biphenyl (1) 1
2,2 '-bis-1,1 '-biaryls (1) 1
2,2'-bis-1,1'-biphenyl (1) 1
2,2′-bis-1, 1′-biaryls (1) 1
2,3-dihydrofuran (1) 1
activation (1) 1
ancillary ligands (1) 1
asymmetric arylation (1) 1
biphenyl series (1) 1
biphep (1) 1
catalysis (1) 1
cationic palladium (1) 1
chemical synthesis (1) 1
chemistry, applied (1) 1
chirality (1) 1
coordination compounds (1) 1
coordination-compounds (1) 1
copper (1) 1
cu complexes (1) 1
delayed fluorescence (1) 1
diamine (1) 1
diels-alder reaction (1) 1
dynamic chirality control (1) 1
electrophosphorescent devices (1) 1
emission (1) 1
enantioselectivity (1) 1
ene reaction (1) 1
fluorescence (1) 1
h nmr chemical shifts (1) 1
h-1 nmr chemical shifts (1) 1
highly efficient (1) 1
iridium complexes (1) 1
ligands (1) 1
light-emitting-diodes (1) 1
neutral (1) 1
nucleophilic substitution (1) 1
optical properties (1) 1
optically-active 2,2'-dihalo-1,1'-binaphthyls (1) 1
organolithium intermediates (1) 1
ortho-lithiation (1) 1
oxide (1) 1
palladium (1) 1
phosphine (1) 1
phosphorescence (1) 1
phosphorescent emitters (1) 1
phosphorus (1) 1
photoluminescence (1) 1
photophysical properties (1) 1
platinum (1) 1
resolution (1) 1
ruthenium (1) 1
series (1) 1
structural analysis (1) 1
synthesis (1) 1
thermal stability (1) 1
trifluoropyruvate (1) 1
triplet emitter (1) 1
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Journal of Organometallic Chemistry, ISSN 0022-328X, 1996, Volume 507, Issue 1, pp. 257 - 261
...) and triphenylphosphine. 2,2′-Bis(diphenylphosphino)biphenyl (1,1′-biphenyl-2,2′-dilbis(diphenylphosphine) ( 1)) can be conveniently prepared by Ullmann coupling of 2-iodophenyldiphenylphosphine oxide and subsequent reduction with trichlorosilane. 
Phosphorus | Organolithium intermediates | Nucleophilic substitution | 2,2′-Bis(diphenylphosphino)biphenyl | ORTHO-LITHIATION | SERIES | OXIDE | nucleophilic substitution | ANALOGS | 2,2'-bis(diphenylphosphino)biphenyl | OPTICALLY-ACTIVE 2,2'-DIHALO-1,1'-BINAPHTHYLS | CHEMISTRY, ORGANIC | organolithium intermediates | phosphorus | CHEMISTRY, INORGANIC & NUCLEAR
Journal Article
Organic Letters, ISSN 1523-7060, 01/2002, Volume 4, Issue 1, pp. 91 - 93
GRAPHICS The racemic Pd complex with the chirally flexible (tropos) biphenylphosphine (BIPHEP) ligand can be resolved with enantiopure... 
CHEMISTRY, ORGANIC | 2,2'-BIS(DIPHENYLPHOSPHINO)BIPHENYL | HETERO-DIELS-ALDER | CATIONIC PALLADIUM(II) | ENE REACTIONS | ENANTIOSELECTIVE HYDROGENATION
Journal Article
Organic Letters, ISSN 1523-7060, 01/2001, Volume 3, Issue 2, pp. 243 - 245
The enantio- and diastereomerically pure metal complex of a chirally flexible BIPHEP ligand is obtained through enantiomer-selective coordination of a... 
CHEMISTRY, ORGANIC | 2,2'-BIS(DIPHENYLPHOSPHINO)BIPHENYL | CATALYSIS | ENANTIOSELECTIVE HYDROGENATION
Journal Article
ADVANCED SYNTHESIS & CATALYSIS, ISSN 1615-4150, 04/2001, Volume 343, Issue 3, pp. 284 - 288
The metal complex of the chirally flexible biphenylphosphine (BIPHEP) exists as an equilibrium between the enantiomeric pairs due to the flexibility of BIPHEP.... 
BIPHEP | ruthenium | 2,2'-BIS(DIPHENYLPHOSPHINO)BIPHENYL | ACTIVATION | CHEMISTRY, ORGANIC | diamine | phosphine | CHEMISTRY, APPLIED | dynamic chirality control
Journal Article
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, ISSN 0008-4042, 02/2006, Volume 84, Issue 2, pp. 93 - 98
The absolute configuration of a series of 3,3'-disubstituted-MeO-BIPHEP derivatives can be determined by the H-1 NMR chemical shift of the methoxyl group when... 
H-1 NMR chemical shifts | BIPHENYL SERIES | asymmetric Heck reaction | 2,2 '-bis(diphenylphosphino)-1,1 '-biaryls | ANALOGS | MeO-BIPHEP derivatives | RESOLUTION | assignment of absolute configuration | ASYMMETRIC ARYLATION | 2,3-DIHYDROFURAN | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
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