Asymmetric catalysis of aldol reactions with chiral lewis bases.
about
Tuning the basicity of ionic liquids for efficient synthesis of alkylidene carbonates from CO2 at atmospheric pressure.Preparative and mechanistic studies toward the rational development of catalytic, enantioselective selenoetherification reactionsDirect β-functionalization of cyclic ketones with aryl ketones via the merger of photoredox and organocatalysis.Investigations Concerning the Syntheses of TADDOL-Derived Secondary Amines and Their Use To Access Novel Chiral Organocatalysts.Current progress in the asymmetric aldol addition reaction.A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations.Magnesium-catalyzed asymmetric direct aldol addition of ethyl diazoacetate to aromatic, aliphatic, and alpha,beta-unsaturated aldehydes.Lewis Base Activation of Lewis Acids - Group 13. In Situ Generation and Reaction of Borenium Ions.Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives.Enantioselective aldol reactions catalyzed by chiral phosphine oxides.Lewis base catalysis of the Mukaiyama directed aldol reaction: 40 years of inspiration and advances.The impact of the Mukaiyama aldol reaction in total synthesis.Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins.Towards Tartaric-Acid-Derived Asymmetric Organocatalysts.2,2,2-Trifluoroacetophenone as an organocatalyst for the oxidation of tertiary amines and azines to N-oxides.Stereoselective synthesis of multiple stereocenters by using a double aldol reaction.Imidazolinium salts as catalysts for the aza-Diels-Alder reaction.Organocatalytic asymmetric synthesis of β(3)-amino acid derivatives.First Isolation and Characterization of the Highly Coordinated Group 14 Enolates: Effects of the Coordination Controls on the Geometry and Tautomerization of Germyl Enolates.Tuning Lewis Acidity by a Transannular pπ -σ* Interaction between Boron and Silicon/Germanium Atoms Supported by a Cage-Shaped Framework.Organic chemistry: catalysts break symmetry.Michael Addition Catalyzed by Chiral Secondary Amine Phosphoramide Using Fluorinated Silyl Enol Ethers: Formation of Quaternary Carbon Stereocenters.Copper-catalyzed retro-aldol reaction of β-hydroxy ketones or nitriles with aldehydes: chemo- and stereoselective access to (E)-enones and (E)-acrylonitriles.The role of synergic interaction in transition state formation for the aldol reaction on a metal oxide catalyst: a DFT investigation.Catalytic Enantioselective Aldol Addition ReactionsOrganocatalytic trifluoromethylation of imines using phase-transfer catalysis with phenoxides. A general platform for catalytic additions of organosilanes to iminesGold Catalyzed Multicomponent Reactions beyond A³ Coupling
P2860
Q33468055-B8459E8F-5732-46C0-A333-B320BD3E11F0Q34310326-567C401C-723B-469C-B42B-62A7992419B6Q34385403-E2A2A03A-51A0-4EA4-8BE0-D1DB5227EC2AQ35360412-5A3CC616-AC00-487F-AE2B-C2A3AFBBC7CBQ35651445-FAE3AAB0-0A41-4CA9-985A-357BCD921EC5Q37102966-764A9668-F64A-4419-BE67-3611480AEE71Q37120147-0E0A5669-C3D4-44FF-8BFA-A773B95D177DQ37386032-79E23449-C9D6-4539-94D6-28CC71B28D4DQ37649015-9D059FA2-C178-4DCD-88B8-FE19693C6303Q38119469-C82493AC-2728-4446-8351-B5320308FAB8Q38120718-5A5C7804-E7C1-4165-8A06-56F4A4C6F27BQ38124790-1C823B69-E389-4B1A-81EE-E425B6376C1CQ38909626-D2076281-283E-475E-8EDE-C48930F052E1Q42029153-A88DE056-1191-4AFA-82AA-7899C4BD470BQ44044671-293F3F7C-1F6A-45F8-9252-61EE10258C95Q45058388-D7A3C96A-882F-4074-AFE0-E171B62FF327Q45212143-9363221B-EE56-43DA-A8A1-9F69AB4BFE40Q46452484-36C03A55-B893-4CF5-8912-075244B9417FQ46523190-BAB5B7E5-67CA-441E-A406-EACBB0513D1CQ48172936-360F0D9A-5C1D-4159-9C70-11538AADA4F4Q48664831-28843860-0F11-4A24-ABAE-4D0CAABCD965Q50278058-88D3D7AD-DC4D-4AB9-AC93-47C2552C8192Q51255307-27FCE5E4-9FD9-4F2D-A0D9-5C483CA4883CQ51814835-500BFD68-0C34-424B-BAE1-A2409523FEAAQ56288446-C8576CFE-DA86-43B9-8989-459A3B2B10D7Q56982691-8784DB40-8C8B-4118-B85A-4C541D04A1CBQ58696556-56BE2D19-35CB-46C6-8149-357A887C88A8
P2860
Asymmetric catalysis of aldol reactions with chiral lewis bases.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@ast
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@en
type
label
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@ast
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@en
prefLabel
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@ast
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@en
P356
P1476
Asymmetric catalysis of aldol reactions with chiral lewis bases.
@en
P2093
Denmark SE
Stavenger RA
P304
P356
10.1021/AR960027G
P407
P577
2000-06-01T00:00:00Z