Asymmetric cyanation of aldehydes, ketones, aldimines, and ketimines catalyzed by a versatile catalyst generated from cinchona alkaloid, achiral substituted 2,2'-biphenol and tetraisopropyl titanate.

Asymmetric cyanation of aldehydes, ketones, aldimines, and ketimines catalyzed by a versatile catalyst generated from cinchona alkaloid, achiral substituted 2,2'-biphenol and tetraisopropyl titanate.

Item
http://www.wikidata.org/entity/Q43272652
Synthesis of unsymmetrical o-biphenols and o-binaphthols via silicon-tethered Pd-catalyzed C-H arylationInterplay of Exciton Coupling and Large-Amplitude Motions in the Vibrational Circular Dichroism Spectrum of Dehydroquinidine.2-Aryl-2-nitroacetates as central precursors to aryl nitromethanes, α-ketoesters, and α-amino acids.Enantioselective cyanoethoxycarbonylation of isatins promoted by a Lewis base-Brønsted acid cooperative catalyst.Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines.A theoretical investigation on the Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate.Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes.Highly efficient asymmetric additions of diethylzinc to aldehydes triply activated by chiral phosphoramide-Zn(II) complexes derived from cinchona alkaloids.Organocatalytic enantio- and diastereoselective cycloetherification via dynamic kinetic resolution of chiral cyanohydrins.Tandem Oxidative Derivatization of Nitrene Insertion Products for the Highly Diastereoselective Synthesis of 1,3-aminoalcohols.Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.A highly enantioselective catalytic Strecker reaction of cyclic (Z)-aldimines.Highly Enantioselective Synthesis of Tertiary Boronic Esters and their Stereospecific Conversion to other Functional Groups and Quaternary StereocentresHydroxynitrile Lyase from Arabidopsis thaliana: Identification of Reaction Parameters for Enantiopure Cyanohydrin Synthesis by Pure and Immobilized Catalyst
P2860

Asymmetric cyanation of aldehydes, ketones, aldimines, and ketimines catalyzed by a versatile catalyst generated from cinchona alkaloid, achiral substituted 2,2'-biphenol and tetraisopropyl titanate.

Item
http://www.wikidata.org/entity/Q43272652
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@en
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@nl
type
label
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@en
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@nl
prefLabel
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@en
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Asymmetric cyanation of aldehy ...... l and tetraisopropyl titanate.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698