Catalyzed Vinylogous Mukaiyama Aldol Reactions with Controlled Enantio- and Diastereoselectivities

Catalyzed Vinylogous Mukaiyama Aldol Reactions with Controlled Enantio- and Diastereoselectivities

Item
http://www.wikidata.org/entity/Q57404844
A convenient enantioselective decarboxylative aldol reaction to access chiral α-hydroxy esters using β-keto acids.Enantioselective iridium-catalyzed vinylogous Reformatsky-aldol reaction from the alcohol oxidation level: linear regioselectivity by way of carbon-bound enolatesThe organocatalytic vinylogous aldol reaction: recent advances.Recent advances in chiral imino-containing ligands for metal-catalyzed asymmetric transformations.Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones.Selective syntheses of Δ(α,β) and Δ(β,γ) butenolides from allylic cyclopropenecarboxylates via tandem ring expansion/[3,3]-sigmatropic rearrangementsCinchona alkaloid/Ti(IV)-catalyzed enantioselective enamine-trifluoropyruvate condensation-cyclization reaction and its application to drug-like heterocycles.Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted butenolides to 3-aroyl acrylates and 1,2-diaroylethylenes.Highly stereoselective directed reactions and an efficient synthesis of azafuranoses from a chiral aziridine.A Simple Tetraminocalix[4]arene as a Highly Efficient Catalyst under "On-Water" Conditions through Hydrophobic Amplification of Weak Hydrogen Bonds.Highly enantioselective synthesis of γ-substituted butenolides via the vinylogous Mukaiyama-Michael reaction catalyzed by a chiral scandium(III)-N,N'-dioxide complex.Diastereo- and enantioselective direct vinylogous Michael addition of γ-substituted butenolides to 2-enoylpyridines catalyzed by chiral bifunctional amine-squaramides.Asymmetric Copper-Catalyzed Vinylogous Mukaiyama Michael Addition of Cyclic Dienol Silanes to Unsaturated α-Keto PhosphonatesCatalytic, Asymmetric Synthesis of Phosphonic γ-(Hydroxyalkyl)butenolides with Contiguous Quaternary and Tertiary Stereogenic CentersMicrowave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles
P2860

Catalyzed Vinylogous Mukaiyama Aldol Reactions with Controlled Enantio- and Diastereoselectivities

Item
http://www.wikidata.org/entity/Q57404844
description
im Februar 2009 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в лютому 2009
@uk
name
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@en
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@nl
type
label
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@en
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@nl
prefLabel
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@en
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
Catalyzed Vinylogous Mukaiyama ...... io- and Diastereoselectivities
@en
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921