(Phosphanyloxazoline)palladium complexes, part I: (Eta3-1,3-dialkylallyl)(phosphanyloxazoline)palladium complexes: X-ray crystallographic studies, NMR investigations, and quantum-chemical calculations.
about
A new modular phosphite-pyridine ligand library for asymmetric Pd-catalyzed allylic substitution reactions: a study of the key Pd-π-allyl intermediates.Quantitative Determination of the Regioselectivity of Nucleophilic Addition to η-Propargyl Rhenium Complexes and Direct Observation of an Equilibrium Between η-Propargyl Rhenium Complexes and RhenacyclobutenesUnusual allylpalladium carboxylate complexes: identification of the resting state of catalytic enantioselective decarboxylative allylic alkylation reactions of ketones.Electronic differentiation competes with transition state sensitivity in palladium-catalyzed allylic substitutions.Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.A superior P-H phosphonite: asymmetric allylic substitutions with fenchol-based palladium catalystsThe reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation.An exceptional P-H phosphonite: biphenyl-2,2'-bisfenchylchlorophosphite and derived ligands (BIFOPs) in enantioselective copper-catalyzed 1,4-additions.Ligand bite governs enantioselectivity: electronic and steric control in Pd-catalyzed allylic alkylations by modular fenchyl phosphinites (FENOPs).Aryl palladium carbene complexes and carbene-aryl coupling reactions.Catalytic Enantioselective and Diastereoselective Allylic Alkylation with Fluoroenolates: Efficient Access to C3-Fluorinated and All-Carbon Quaternary Oxindoles.Origin of Selectivity of Tsuji-Trost Allylic Alkylation of Lactones: Highly Ordered Transition States with Lithium-Containing EnolatesEnantioselective and Diastereoselective Tsuji-Trost Allylic Alkylation of Lactones: An Experimental and Computational Study
P2860
Q34538796-B24EC193-3FA5-4B3B-8ADD-907BD52140E9Q37088983-38791BC5-3D56-417F-A1C7-C299A4B06D60Q40874273-F536488D-F767-49E5-805B-4A47D6471623Q41952911-2C77DD14-7BAC-44EE-8475-A1E4E013FFDFQ42182848-F505CC39-D9B8-47C7-99CF-F56A8D8ED362Q42408270-C61D2688-176E-4276-8D0C-8D82CDB8E17AQ42534222-22137B07-B756-4504-AB50-C3383B4D9DBEQ43239128-BA14E947-6F74-463F-BD74-6332AB664038Q45066393-56BE3CFB-6264-458A-9FC3-873BC9FCC72AQ45232560-516988A6-41A9-4577-B5E4-8631615C10E4Q50326087-1A8D14AD-B533-4FFF-AB20-8C298B50AF9DQ57397763-C62B33C6-ED5D-4DD3-A7F3-52882938A4CBQ57397782-BFD6976A-88FD-4F8E-9AE3-7DD52955A8EA
P2860
(Phosphanyloxazoline)palladium complexes, part I: (Eta3-1,3-dialkylallyl)(phosphanyloxazoline)palladium complexes: X-ray crystallographic studies, NMR investigations, and quantum-chemical calculations.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@en
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@nl
type
label
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@en
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@nl
prefLabel
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@en
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@nl
P2093
P1476
(Phosphanyloxazoline)palladium ...... quantum-chemical calculations.
@en
P2093
Goldfuss B
Helmchen G
Reggelin M
Rominger F
P304
P356
10.1002/1521-3765(20011119)7:22<4913::AID-CHEM4913>3.0.CO;2-7
P407
P577
2001-11-01T00:00:00Z