About: Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles

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About: Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles Goto Sponge NotDistinct Permalink

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description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2018 (uk) article scientifique publié en 2018 (fr) im Juni 2018 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q59769451-1F30EBB1-209A-4FA8-82C0-BC9B1CF2DA31
publication date	2018-06-25 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59769451-C103B427-4698-49A8-AB27-DA19EC445026
language of work or name	English
cites work	wds:Q59769451-05BB76DF-0963-46BA-AA1C-A676A72F2671 wds:Q59769451-05E0AC51-7147-4BFC-8F9E-FFD04BDA3B0F wds:Q59769451-0ECD7430-B559-4CBB-BF3D-9565332348EA wds:Q59769451-0ED5A221-F8FC-4910-818A-1CDC482A03F2 wds:Q59769451-0FA35198-D28A-4334-B1FE-7A82F506F4CD wds:Q59769451-1A9DF5BD-DAD0-4C3C-9663-42735DAB1BD2 wds:Q59769451-1FBE6942-7017-4554-A7B1-30BBF48F4E36 wds:Q59769451-2B033BEA-90DC-42B2-9A62-C84617F26B64 wds:Q59769451-2CB71340-A0ED-4817-B919-B5864C179561 wds:Q59769451-316E8F2E-82A4-4609-AB7D-CB69FE54A60B wds:Q59769451-347D8E4E-C665-4214-B8AC-12AED57D6C97 wds:Q59769451-3B2A3F30-4241-40FE-B0DB-81F368282DA8 wds:Q59769451-43596E59-3D7D-4872-86B9-F0FB104153B0 wds:Q59769451-4525909D-0B57-4912-AF88-CA4BD169E08C wds:Q59769451-45FCE34E-E63D-4B53-8D24-3C418A4BBF69 wds:Q59769451-465D92CB-BC1F-481E-BF74-2F73AE308B61 wds:Q59769451-4920D3C3-78AF-4128-9A7A-D5D55CE9D6EB wds:Q59769451-4C728647-1211-46C5-9125-F02D763A7201 wds:Q59769451-4F3E0ECE-C3A2-4E06-A6E6-2DDC7E4858A6 wds:Q59769451-54157990-01CB-4A33-B471-A0CA029BFB65 wds:Q59769451-5FDCE6EA-5D25-4320-9594-C5D519D5638B wds:Q59769451-79BF9A40-6993-4060-8BC2-20CE98DC9214 wds:Q59769451-7C98378A-8BA3-4F87-B544-F3590728ABCB wds:Q59769451-8D3CBEE0-9501-4BDE-B1B3-0E1FECA739D1 wds:Q59769451-8F22C279-4B09-42FE-9566-B38921CFECB6 wds:Q59769451-9EA8F0FB-8118-4771-A945-969AF2AAE259 wds:Q59769451-A1840101-2862-48EE-9B54-1044AB9C0B8E wds:Q59769451-A47A5D20-F2A7-4ECB-AF4D-9C9F8CFBB101 wds:Q59769451-A73F158A-9185-4190-B70D-7B7F294F8CD7 wds:Q59769451-A8207B42-3EA4-4A7B-906F-DE2FC7C70587 wds:Q59769451-AAEFB9E5-2972-4C75-8AC8-2E01B880D3DA wds:Q59769451-C0C316F6-94CA-4305-B37B-C4BE6A681792 wds:Q59769451-C97C817F-E5D4-4ACD-8ECB-4CBA44976743 wds:Q59769451-E8B9AB83-81BA-47C5-B427-1E1034A487E9 wds:Q59769451-EDD4CB29-2981-465C-8048-7AEF3B7DDBFD wds:Q59769451-F67C55DC-CB47-46A1-81EF-CB042499DA7A
cites work	Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis Asymmetric transition-metal-catalyzed allylic alkylations: applications in total synthesis Transition metal-catalyzed decarboxylative allylation and benzylation reactions Benzotetramisole: A Remarkably Enantioselective Acyl Transfer Catalyst Asymmetric Transition Metal-Catalyzed Allylic Alkylations Synergistic Catalysis: A Powerful Synthetic Strategy for New Reaction Development A Survey of the Role of Noncovalent Sulfur Interactions in Drug Design. Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. Origin of Enantioselectivity in Benzotetramisole-Catalyzed Dynamic Kinetic Resolution of Azlactones 2-furyl phosphines as ligands for transition-metal-mediated organic synthesis An isothiourea-catalyzed asymmetric [2,3]-rearrangement of allylic ammonium ylides The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation Combining transition metal catalysis and organocatalysis--an update From bifunctional to trifunctional (tricomponent nucleophile-transition metal-lewis acid) catalysis: the catalytic, enantioselective α-fluorination of acid chlorides Benzotetramisole-catalyzed dynamic kinetic resolution of azlactones Asymmetric organocatalysis combined with metal catalysis: concept, proof of concept, and beyond Synthesis of N-carbobenzoxyamino acid and peptide pentafluorophenyl esters as intermediates in peptide synthesis Asymmetric [4+2] Annulation of C1 Ammonium Enolates with Copper-Allenylidenes. Combinations of Aminocatalysts and Metal Catalysts: A Powerful Cooperative Approach in Selective Organic Synthesis. Iridium-Catalyzed Diastereo-, Enantio-, and Regioselective Allylic Alkylation with Prochiral Enolates Stereodivergent Allylic Substitutions with Aryl Acetic Acid Esters by Synergistic Iridium and Lewis Base Catalysis The Origin of Chalcogen-Bonding Interactions. Catalytic, asymmetric reactions of ketenes and ketene enolates. Tandem Palladium and Isothiourea Relay Catalysis: Enantioselective Synthesis of α-Amino Acid Derivatives via Allylic Amination and [2,3]-Sigmatropic Rearrangement. Lewis Base/Copper Cooperatively Catalyzed Asymmetric α-Amination of Esters with Diaziridinones. Enantioselective Cascade Reaction for Synthesis of Quinolinones through Synergistic Catalysis Using Cu-Pybox and Chiral Benzotetramisole as Catalysts. Kinetic resolution of N-acyl-β-lactams via benzotetramisole-catalyzed enantioselective alcoholysis Uniting C1-Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α-Allylation of Aryl Acetic Acid Esters Towards perfect catalytic asymmetric synthesis: dual activation of the electrophile and the nucleophile Isothiourea-mediated asymmetric functionalization of 3-alkenoic acids Catalytic Enantioselective [2,3]-Rearrangements of Allylic Ammonium Ylides: A Mechanistic and Computational Study Aryloxide-Facilitated Catalyst Turnover in Enantioselective α,β-Unsaturated Acyl Ammonium Catalysis A surprising mechanistic "switch" in Lewis acid activation: a bifunctional, asymmetric approach to alpha-hydroxy acid derivatives Enantioselective nucleophile-catalyzed synthesis of tertiary alkyl fluorides via the α-fluorination of ketenes: synthetic and mechanistic studies Controlling chemoselectivity in vinyl and allylic C-X bond activation with palladium catalysis: a pK(a)-based electronic switch Allylic substitution versus Suzuki cross-coupling: capitalizing on chemoselectivity with bifunctional substrates
author name string	wds:Q59769451-2BD127A9-34E1-4553-83CF-C38729C2C1B2 wds:Q59769451-9CD3A26C-8C09-44B4-902D-D4F24F2C3703 wds:Q59769451-FC891BE9-E69A-4FB2-97EB-278E6DF594ED
author name string	Kevin J Schwarz Colin M Pearson Gabriel A Cintron-Rosado
rdfs:label	Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (en) Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (nl)
skos:prefLabel	Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (en) Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (nl)
name	Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (en) Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (nl)
author	wds:Q59769451-47B300F4-F57F-4601-A41B-09991C905974 wds:Q59769451-B0D6C97D-D4C9-4593-BBB7-22D887BE953C
author	Peng Liu Thomas N Snaddon
title	wds:Q59769451-0A8B37B5-0DAC-4866-A4B9-AA86F13FCC22
title	Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles (en)
page(s)	wds:Q59769451-857F0D38-B89D-4EE4-9B05-281E6424CF31

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