Palladium(II)-catalyzed asymmetric hydrophosphination of enones: efficient access to chiral tertiary phosphines.
about
Palladacycle catalyzed asymmetric P-H addition of diarylphosphines to N-enoyl phthalimides.Recent developments in metal catalyzed asymmetric addition of phosphorus nucleophiles.Our Odyssey with Functionalized Chiral Phosphines: From Optical Resolution to Asymmetric Synthesis to Catalysis.Palladacycle promoted base controlled regio- and enantioselective hydrophosphination of 2-pyridylacrylate/amide and the cytotoxicity of their gold complexes.Synthesis, structural characterisation and stereochemical investigation of chiral sulfur-functionalised N-heterocyclic carbene complexes of palladium and platinum.Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to α,β,γ,δ-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups.Terminal phosphanido rhodium complexes mediating catalytic P-P and P-C bond formation.Azetidine-derived dinuclear zinc catalyzed asymmetric phospha-Michael addition of dialkyl phosphite to α,β-unsaturated carbonyl compounds.Nickel catalyzed enantioselective hydroarsination of nitrostyrene.Challenges in Catalytic Hydrophosphination.Mechanistic insights into the role of PC- and PCP-type palladium catalysts in asymmetric hydrophosphination of activated alkenes incorporating potential coordinating heteroatoms.Computational and carbon-13 NMR studies of Pt-C bonds in P-C-P pincer complexes.Pd-catalyzed enantiodivergent and regiospecific phospha-Michael addition of diphenylphosphine to 4-oxo-enamides: efficient access to chiral phosphinocarboxamides and their analogues.Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters - efficient control of reactivity, stereo- and regio-selectivity.Enantioselective phospha-Michael addition of diarylphosphines to β,γ-unsaturated α-ketoesters and amides.A tandem Heck-aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected amines.Domino cyclization-alkylation protocol for the synthesis of 2,3-functionalized indoles from o-alkynylanilines and allylic alcohols.Highly efficient asymmetric Michael addition of diaryl phosphine oxides to α,β-unsaturated N-acylated oxazolidin-2-ones.Chiral palladacycle catalysts generated on a single-handed helical polymer skeleton for asymmetric arylative ring opening of 1,4-epoxy-1,4-dihydronaphthalene.Catalyst- and solvent-free hydrophosphination and multicomponent hydrothiophosphination of alkenes and alkynesSolvent- and catalyst-free regioselective hydrophosphanation of alkenes
P2860
Q35252269-E5326599-10ED-4EB3-9BE1-00EE74FE749AQ37968541-09608BD1-0D8C-4E7A-A9CD-EBD4C5C6EB29Q38561051-5BF3354A-ED9A-40D7-9909-CBF1EB24E664Q38833790-54DD5A1F-DE42-4966-BE59-1DB19C7BE397Q44630380-6BC5CB3A-7854-49C6-B2B7-995CC15F0F11Q45012838-E04B92CA-980A-4826-B3DC-3B3D6C704EF7Q46812370-7A37A463-34B5-4824-ADF8-D0792E7C22C7Q47379280-5E37B62A-4844-4ECA-911C-2E012991CCECQ47851029-E19F5A98-9C77-4BA9-9887-1319A74CD0A8Q48163247-C369997D-0276-4629-ABA2-18B43BA026CBQ50599721-592CB6A4-DB81-497C-A0D8-894A1456592AQ50789156-25C4B474-E495-4502-B7C7-4A6467B7E298Q50960065-60D3F552-C67F-444A-AB8B-A582EE53C17CQ51009374-8F6A6B5D-03F7-4B9C-9306-08FF3722C536Q51073845-5EAF3A8E-05CE-4A26-9FD6-1082F0D709CBQ51343820-4AE82B75-D1D8-4C59-A5A0-0299D2D6D61AQ51376395-3477A0C1-E271-4A5B-96B4-66DE5F84EAA9Q52735284-4B67C82F-F92A-417C-AF12-986A91E31743Q53435595-A07D9FBD-E9FF-4B98-8C22-27E8503E8A30Q57832581-B594D4DB-02D6-46C4-A2C8-B88034BAC661Q57832612-5B2ED522-0562-4C0A-83D5-E31852F49714
P2860
Palladium(II)-catalyzed asymmetric hydrophosphination of enones: efficient access to chiral tertiary phosphines.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@ast
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@en
type
label
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@ast
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@en
prefLabel
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@ast
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines.
@en
P2093
P356
P1476
Palladium(II)-catalyzed asymme ...... to chiral tertiary phosphines
@en
P2093
Pak-Hing Leung
Yinhua Huang
Yongxin Li
P304
P356
10.1039/C0CC00925C
P407
P577
2010-08-23T00:00:00Z