about
Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural ProductAltered retinoid homeostasis catalyzed by a nicotine metabolite: implications in macular degeneration and normal developmentGeneration of α,β-unsaturated iminium ions by laser flash photolysis.C-H bond functionalization via hydride transfer: Lewis acid catalyzed alkylation reactions by direct intramolecular coupling of sp3 C-H bonds and reactive alkenyl oxocarbenium intermediates.Synthesis of Oxazolidinone and Tosyl Enamines by Tertiary Amine CatalysisBroader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation.Origin of stereoselectivity in the imidazolidinone-catalyzed reductions of cyclic alpha,beta-unsaturated ketones.Transfer hydrogenation with Hantzsch esters and related organic hydride donors.Catalytic selective synthesis.Asymmetric ion-pairing catalysis.Asymmetric counteranion-directed catalysis: concept, definition, and applications.Asymmetric organocatalysis at the service of medicinal chemistryKinetic Resolution of Azomethine Imines by Brønsted Acid Catalyzed Enantioselective Reduction.Recent advances in organocatalytic enantioselective transfer hydrogenation.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions.The organocatalytic three-step total synthesis of (+)-frondosin B.A quantitative approach to nucleophilic organocatalysis.Synthesis, SAR, and Pharmacological Characterization of Brain Penetrant P2X7 Receptor AntagonistsEnantioselective alpha-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway.Waste as catalyst: tandem Wittig/conjugate reduction sequence to α-CF3 γ-keto esters that uses Ph3PO as catalyst for the chemoselective conjugate reduction.Enantioselective total synthesis of atpenin A5.A classical but new kinetic equation for hydride transfer reactions.Iminium Catalysis inside a Self-Assembled Supramolecular Capsule: Modulation of Enantiomeric Excess.A Stereoconvergent Cyclopropanation Reaction of Styrenes.CuH-Catalyzed Asymmetric Reduction of α,β-Unsaturated Carboxylic Acids to β-Chiral Aldehydes.Asymmetric Traceless Petasis Borono-Mannich Reactions of Enals: Reductive Transposition of Allylic Diazenes.Iridium-catalyzed asymmetric hydrogenation of 3,3-disubstituted allylic alcohols in ethereal solvents.Asymmetric Diels-Alder Reaction of α-Substituted and β,β-Disubstituted α,β-Enals via Diarylprolinol Silyl Ether for the Construction of All-Carbon Quaternary Stereocenters.Comparative characterization of novel ene-reductases from cyanobacteria.Bioinspired organocatalytic asymmetric reactions.Enantioselective and diastereoselective azo-coupling/iminium-cyclizations: a unified strategy for the total syntheses of (-)-psychotriasine and (+)-pestalazine B.Immobilization of MacMillan catalyst via controlled radical polymerization: catalytic activity and reuseStereoselectivity through a network of non-classical CH weak interactions: a prospective study of a bicyclic organocatalytic scaffoldAb initio quantum chemical and ReaxFF-based study of the intramolecular iminium–enamine conversion in a proline-catalyzed reactionOn the Roles of Protic Solvents in Imidazolidinone-Catalyzed TransformationsOrganocatalysis: Key Trends in Green Synthetic Chemistry, Challenges, Scope towards Heterogenization, and Importance from Research and Industrial Point of View
P2860
Q26749672-2616DD00-E382-4F2D-9D30-F831360595B9Q33906776-57E17923-A969-44FA-A108-ABC60FE5F058Q34013164-696BAD2C-CDB4-49DD-99D2-A5FCF0C3760FQ34198744-98CF96DC-3CA4-4EFE-B52C-92A5B4FD50D5Q34687122-4D8DB8FE-9B35-478D-B091-D4696F4D196DQ37254438-EC75002A-CB64-4336-99C2-1CD686E1852CQ37362531-8DCE1F4A-969F-4D1E-A6DF-D819E784C060Q37979197-21AEC10D-5380-442C-A432-FC7EF7FBCC08Q38046517-4921B23C-F548-4A55-B223-BA4DBD6FAA7CQ38063471-74D390B7-6A94-42B0-9A16-19C0CF64ABBCQ38070995-1D615FA4-7E9F-4781-A525-E7A4ADE8EE5BQ38223762-F73CAF74-5586-4BF6-A894-4BFFA5E49B04Q38420625-BE77C4B7-4BDA-4913-B347-0A9A28BEC70CQ38754364-91DA69E7-8A42-4D25-97B0-9D9CE3CE7A35Q39240715-2A62799D-4A5A-47C2-AFDD-2C645C8F4729Q39442487-D05578CA-DF9D-492D-A13B-753F64CB5008Q40730595-D96C6B80-64FE-4518-B733-B8340D8B1054Q42084604-B02E0D75-79A6-405D-A9A5-8D4A0B0DC7D1Q42430715-A904D3B7-35A9-4E04-80D1-692ADC154A82Q42578835-B1554ED6-1213-441A-8122-EB41F17BD9DFQ43434792-E3ECD0AF-F6DC-4E48-8D84-B9CF1A8935B5Q44184140-FCFA160C-5F3E-4E31-A500-DCB40FD09905Q45003942-DD2D0C42-DD3C-4D88-8B39-8161040FA1BDQ46538005-C0D765BE-7DF0-4BE0-BF51-3F7B8E31E101Q48146699-CD0D24F9-7A3D-401A-AF1C-985B4F66B4AAQ48336859-D4F91C3B-5AA3-4488-B7C0-8C99C29EBA4EQ48353756-68244D84-96BD-49DA-844D-0449DFA8A8A6Q50462410-ADD74C45-C455-4CCE-83D5-A17AF1655648Q51133780-3E68620E-4F0D-4240-ACFE-9B1D8FA447CFQ51541199-4E026824-3AB0-4DA9-AB2D-7127D2D7E74EQ54344629-CB3E5F1E-FAED-4996-917F-386D28DD1BB4Q55461620-CBEECDDB-9BE5-4FF9-B48F-6B9EC874656FQ57367807-3E862FB7-A02B-4EC7-A1FE-09DF96097686Q57400161-3637EEC0-CB9A-4A36-AD3A-A9B584D10680Q57770685-77650D11-1FC5-45D1-BEA6-39CC2BE3AA73Q58486676-84924866-1D45-4CE3-977C-239129695C11Q59055390-D6624D00-E30C-4F0E-AFB4-7ED281A948D9
P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
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
name
Enantioselective organocatalytic hydride reduction
@ast
Enantioselective organocatalytic hydride reduction
@en
Enantioselective organocatalytic hydride reduction
@nl
type
label
Enantioselective organocatalytic hydride reduction
@ast
Enantioselective organocatalytic hydride reduction
@en
Enantioselective organocatalytic hydride reduction
@nl
prefLabel
Enantioselective organocatalytic hydride reduction
@ast
Enantioselective organocatalytic hydride reduction
@en
Enantioselective organocatalytic hydride reduction
@nl
P2093
P3181
P356
P1476
Enantioselective organocatalytic hydride reduction
@en
P2093
David W C MacMillan
Jamison B Tuttle
Stéphane G Ouellet
P3181
P356
10.1021/JA043834G
P407
P577
2005-01-12T00:00:00Z