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chemistry, inorganic & nuclear (27) 27
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2011, RSC catalysis series, ISBN 1849731233, Volume no. 7., xvii, 501
This book provides comprehensive coverage of the application of P-stereogenic ligands in homogeneous catalysis.. 
Enantioselective catalysis | Ligands | Science | General | Chemistry | Physical & Theoretical
Book
2011, RSC catalysis series, ISBN 9781849731232, Volume no. 7
Web Resource
CATALYSIS SCIENCE & TECHNOLOGY, ISSN 2044-4753, 10/2019, Volume 9, Issue 20, pp. 5504 - 5561
Journal Article
ISSN 2044-4753, 10/2019, Volume 9, Issue 2, pp. 554 - 5561
Secondary phosphine oxides present tautomeric equilibrium between the pentavalent oxide form (SPO) and the trivalent phosphinous acid (PA). This dichotomy is... 
Journal Article
Dalton Transactions, ISSN 1477-9226, 01/2018, Volume 47, Issue 15, pp. 5366 - 5379
Both enantiomers of the optically pure Secondary Phosphine Oxide (SPO) t-BuMeP(O)H (1) have been obtained by deboronation of phosphinous acid-borane... 
Gold | Ruthenium | Palladium | Iridium | Coordination compounds | Enantiomers | Chemical synthesis | Crystallography | Phosphine oxide | Crystal structure
Journal Article
Dalton Transactions, ISSN 1477-9226, 01/2017, Volume 46, Issue 45, pp. 15865 - 15874
The reaction of the acetylacetonates [(η5-C5Me5)M(acac)Cl] with (SP)-[HMaxPhos][BF4] afforded cationic complexes with the formula... 
Iridium compounds | Ruthenium | Rhodium | Chirality | Ligands | Cations | Iridium | Isomers | Crystal structure | Adducts
Journal Article
ISSN 1477-9226, 4/2018, Volume 47, Issue 15, pp. 5366 - 5379
Both enantiomers of the optically pure Secondary Phosphine Oxide (SPO) t -BuMeP(O)H ( 1 ) have been obtained by deboronation of phosphinous acid-borane t... 
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 09/2019, Volume 896, pp. 51 - 58
Reactions of optically pure -stereogenic -tolyl substituted phosphines with [RuCl ( -cymene)] afforded the corresponding -coordinated ruthenium(II) dichlorides... 
Reduction of ketones | Ruthenium | P-stereogenic phosphines | Asymmetric catalysis | Cyclometallated complexes | IMINES | CHEMISTRY, ORGANIC | TRANSFER HYDROGENATION | CATALYST | ALLYLPALLADIUM COMPLEXES | CHEMISTRY, INORGANIC & NUCLEAR | H BOND ACTIVATION | LIGANDS | AMINES | PHOSPHINES | ASYMMETRIC HYDROVINYLATION | Aromatic amines | Catalysis
Journal Article
European Journal of Inorganic Chemistry, ISSN 1434-1948, 09/2016, Volume 2016, Issue 25, pp. 4054 - 4065
The synthesis of 14 new optically pure C1‐symmetric phosphane–phosphinite (1–4), phosphane–phosphite (5–9) and phosphane–phosphorodiamidite (10–14) ligands is... 
P ligands | Palladium | Asymmetric catalysis | Allylic substitution | RHODIUM | PALLADIUM COMPLEXES | STYRENE | HYDROVINYLATION | CHEMISTRY, INORGANIC & NUCLEAR | IRIDIUM COMPLEXES | ENANTIOSELECTIVE HYDROGENATION | HYDROFORMYLATION REACTIONS | PURE | METAL-COMPLEXES | MONODENTATE PHOSPHINES | Substitution reactions | Enantiomers | Diastereomers | Ligands | Dimethyl | Cationic | Coordination compounds | Conversion | Alkylation
Journal Article
Journal of Molecular Catalysis A: Chemical, ISSN 1381-1169, 11/2012, Volume 363-364, pp. 49 - 57
Five Ru(II) neutral complexes C of the type [RuCl (η -arene)(P)] (P = monodentate phosphorus ligand) have been prepared: C1 (arene = p-cymene, P = PPh ); C2... 
Induction period | Transfer hydrogenation | Acetophenone reduction | Ruthenium arene complexes
Journal Article
ISSN 1477-9226, 5/2016, Volume 45, Issue 2, pp. 8513 - 8531
The synthesis via phosphine-boranes of 13 new optically pure P -stereogenic diarylphosphines P(Het)PhR (Het = 4-dibenzofuranyl (DBF), 4-dibenzothiophenyl... 
Journal Article
Organometallics, ISSN 0276-7333, 10/2015, Volume 34, Issue 20, pp. 4989 - 4993
The asymmetric Pauson–Khand reaction catalyzed by [Rh­(COD)­(MaxPHOS)]­BF4 is described. Several 1,6-enynes have been chosen as model substrates affording... 
MAXPHOS | CHEMISTRY, ORGANIC | CYCLIZATION | COMPLEXES | CHEMISTRY, INORGANIC & NUCLEAR
Journal Article
Catalysts, ISSN 2073-4344, 09/2019, Volume 9, Issue 10, p. 811
The study of the reactivity of three 2-phenyl-3H-indole ligands of general formulae C8H3N-2-(C6H4-4-R1)-3-NOMe-5-R2 (1) [with R1 = H, R2 = OMe (a); R1 = R2 = H... 
Ligands | Lligands | Compostos orgànics | Catàlisi homogènia | Homogeneous catalysis | Organic compounds | homogeneous catalysis | 2-phenyl-3h-indoles | solution behavior | computational studies | pd-allyl complexes
Journal Article
RSC Catalysis Series, ISSN 1757-6725, 2010, pp. 1 - 521
Conference Proceeding
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