Thiourea-catalyzed enantioselective cyanosilylation of ketones.
about
Structural optimization of thiourea-based bifunctional organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones.Chiral poly-rare earth metal complexes in asymmetric catalysis.Chiral imine copper chloride-catalyzed enantioselective desymmetrization of 2-substituted 1,2,3-propanetriols.Effect of carbonates/phosphates as nucleophilic catalysts in dimethylformamide for efficient cyanosilylation of aldehydes and ketones.Catalytic enantioselective olefin metathesis in natural product synthesis. Chiral metal-based complexes that deliver high enantioselectivity and moreNovel bifunctional sulfonamides catalyze an enantioselective conjugate addition.Asymmetric counteranion-directed Lewis acid organocatalysis for the scalable cyanosilylation of aldehydes.Enantioselective total synthesis of (-)-acylfulvene and (-)-irofulven.The Cyanation of Prochiral Aldehydes with Chiral Copper Complexes of R-(+)/S-(-) -α-Ethylphenyl Amine in Methanol.Synthesis and evaluation of new guanidine-thiourea organocatalyst for the nitro-Michael reaction: Theoretical studies on mechanism and enantioselectivity.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.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.What is the mechanism of amine conjugate additions to pyrazole crotonate catalyzed by thiourea catalysts?Metal free mild and selective aldehyde cyanosilylation by a neutral penta-coordinate silicon compound.Crystal engineering with urea and thiourea hydrogen-bonding groups.Organocatalytic enantio- and diastereoselective cycloetherification via dynamic kinetic resolution of chiral cyanohydrins.Study on the Catalytic Behavior of Bifunctional Hydrogen-Bonding Catalysts Guided by Free Energy Relationship Analysis of Steric Parameters.Beyond Hydrofunctionalisation: A Well-Defined Calcium Compound Catalysed Mild and Efficient Carbonyl Cyanosilylation.A dramatic synergistic effect of a flexible achiral linker on a rigid chiral cis-1,2-diamine bifunctional organocatalyst.Asymmetric sequential Au(i)/chiral tertiary amine catalysis: an enone-formation/cyanosilylation sequence to synthesize optically active 3-alkenyloxindoles from diazooxindoles.Toward a practical and waste-free synthesis of thioureas in water.Enantioselective Cyanosilylation of Ketones with Lithium(I) Dicyanotrimethylsilicate(IV) Catalyzed by a Chiral Lithium(I) Phosphoryl Phenoxide.Electrochemical Acetylcholine Chloride Biosensor Using an Acetylcholine Esterase BiomimicOrganocatalysis: Key Trends in Green Synthetic Chemistry, Challenges, Scope towards Heterogenization, and Importance from Research and Industrial Point of View
P2860
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P2860
Thiourea-catalyzed enantioselective cyanosilylation of ketones.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Thiourea-catalyzed enantioselective cyanosilylation of ketones.
@en
type
label
Thiourea-catalyzed enantioselective cyanosilylation of ketones.
@en
prefLabel
Thiourea-catalyzed enantioselective cyanosilylation of ketones.
@en
P2860
P356
P1476
Thiourea-catalyzed enantioselective cyanosilylation of ketones.
@en
P2093
Douglas E Fuerst
Eric N Jacobsen
P2860
P304
P356
10.1021/JA052511X
P407
P577
2005-06-01T00:00:00Z