about
Mechanistic, crystallographic, and computational studies on the catalytic, enantioselective sulfenofunctionalization of alkenes.Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groupsCatalytic Asymmetric Additions of Carbon-Centered Nucleophiles to Nitrogen-Containing Aromatic HeterocyclesScaffolding Catalysis: Expanding the Repertoire of Bifunctional Catalysts.Enantioselective protonation.Lewis base catalyzed, enantioselective, intramolecular sulfenoamination of olefinsPhosphine-catalyzed [4+2] annulations of 2-alkylallenoates and olefins: synthesis of multisubstituted cyclohexenesEnantioselective boronate additions to N-acyl quinoliniums catalyzed by tartaric acidChiral phosphines in nucleophilic organocatalysisDiscovering New Reactions with N-Heterocyclic Carbene Catalysis.Preparative and mechanistic studies toward the rational development of catalytic, enantioselective selenoetherification reactionsPHOSPHINE-CATALYZED [3 + 2] ANNULATION: SYNTHESIS OF ETHYL 5-(tert-BUTYL)-2-PHENYL-1-TOSYL-3-PYRROLINE-3-CARBOXYLATEPhosphine-Catalyzed [3+2] and [4+3]Annulation Reactions of C,N-Cyclic Azomethine Imines with AllenoatesMultifunctional organoboron compounds for scalable natural product synthesis.Isolation of a C5-deprotonated imidazolium, a crystalline "abnormal" N-heterocyclic carbene.Enantioselective dichlorination of allylic alcohols.Phosphine-catalyzed annulations of azomethine imines: allene-dependent [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] pathways.Catalytic asymmetric thiofunctionalization of unactivated alkenes.Investigations Concerning the Syntheses of TADDOL-Derived Secondary Amines and Their Use To Access Novel Chiral Organocatalysts.Kinetic resolution of secondary alcohols using amidine-based catalysts.One-pot phosphine-catalyzed syntheses of quinolinesCatalytic, asymmetric halofunctionalization of alkenes--a critical perspective.Lewis base catalyzed enantioselective additions of an N-silyl vinylketene imine.Catalytic, enantioselective, intramolecular carbosulfenylation of olefins.Axial preferences in allylation reactions via the Zimmerman-Traxler transition state.Hypervalent surface interactions for colloidal stability and doping of silicon nanocrystalsA dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations.Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis.PHOSPHINE-CATALYZED [4+2] ANNULATION: SYNTHESIS OF ETHYL 6-PHENYL-1-TOSYL-1,2,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLATE.The interplay of invention, discovery, development, and application in organic synthetic methodology: a case study.Impact of solvent polarity on N-heterocyclic carbene-catalyzed beta-protonations of homoenolate equivalentsEnantioselective desymmetrization of cyclohexadienones via an intramolecular Rauhut-Currier reaction of allenoates.Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities.Lewis Base Activation of Lewis Acids - Group 13. In Situ Generation and Reaction of Borenium Ions.Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Preparative and stereochemical aspects.General approach to the synthesis of the chlorosulfolipids danicalipin A, mytilipin A, and malhamensilipin A in enantioenriched form.Diversity of Secondary Structure in Catalytic Peptides with β-Turn-Biased SequencesEnantioselective silyl protection of alcohols promoted by a combination of chiral and achiral Lewis basic catalysts.Asymmetric Cu(II) catalyses for cycloaddition reactions based on π-cation or n-cation interactions.
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Q27312443-2624C2AC-5136-409F-812F-250F88960BEAQ28817194-553C564B-2988-4DBC-A834-A42076A338ADQ30052374-AE450071-72CC-4904-AFE2-CD779EA3DDECQ30414436-8F69004E-53CA-42F0-9EE4-D6159A54EC70Q33812467-5B2D07FD-F3F9-47EB-A761-B454B1BA01DDQ33816452-37CD904F-6CF9-44F2-BF21-8ACC02F847F7Q34004474-03DB2CB6-A822-4FF2-B4C8-4DED898A6856Q34069939-D425541A-FEBD-4138-AC4C-77E1230A269DQ34212163-26CAD09D-2B2F-4D90-9A46-CA2C9DCD248AQ34284871-329D725C-F668-4FA5-A541-56C1B7F7CF60Q34310326-30FB9A4D-252A-46B5-ADA2-00E0DE855482Q34637917-8BB78961-C00D-43BD-88B9-9E8BDBAEF734Q34706915-5C5FF17B-45B7-415C-96BE-728DD73D33C6Q34712211-D35006B9-D826-4CA9-934B-F7A762DB34A7Q35012021-D6A21367-E245-4960-8FB3-D282673681E1Q35021046-C7156A46-05FE-4DD6-B00E-9677F8B2CC52Q35184786-B53C3231-44D2-4FA9-B32C-CC6814280F45Q35277888-A8E545E9-97A6-45C1-8A7C-8218766CD18EQ35360412-D2E0B257-2A4F-49E2-8CBC-6DE47B14FFFFQ35792784-AE33FAC8-D812-43C7-B05B-D6CE4BBB200EQ36283901-F53F77BF-B42B-445F-8334-48280971EEECQ36485386-3CD81227-3B33-448F-BD29-1C63EB0BE899Q36486752-C8DBF5EB-2EC2-40E9-8F3B-8AA96E8C8D6BQ36909354-CE6BB122-BF3B-4492-87D1-E47600D83B92Q37022106-026A8AD5-51E1-4326-AC6F-21F2909519B9Q37064923-B3504260-53DD-44C2-82B8-F02379E1FDB4Q37102966-40BEA29C-564A-4720-B70C-35C13072374DQ37263721-FCE3C761-8966-47A2-96E5-F0610C3A48C7Q37271990-1D38A232-4901-4020-A21B-0EC187EECC02Q37313944-206636F9-50EA-467D-82A7-BCF9898C1481Q37323691-925CE04F-723B-41C6-B751-BAC763FB3C80Q37329798-146077A3-4761-4E3B-8484-460BCDC2D9A9Q37353359-9569214E-7F8E-4686-AAB6-0C27B7BF4E19Q37386032-604ECA16-BB1D-415F-8393-CD148E2220CCQ37552203-96285799-9413-46F3-A7EA-95BE6D486B20Q37552236-2EB72860-1C38-4228-B04C-D1ED082C6D42Q37637645-602F3F8C-05A0-429B-954C-C94A314DD77FQ37646524-B8AF45DB-0A78-49B7-974E-82F6BBA633CAQ37726953-975159D9-F387-4644-96F4-93F30F49019FQ37785751-FE94AEC6-164B-4538-B00A-3CA64641EB1D
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description
article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в лютому 2008
@uk
ലേഖനം
@ml
name
Lewis Base Catalysis in Organic Synthesis
@en
Lewis Base Catalysis in Organic Synthesis
@nl
type
label
Lewis Base Catalysis in Organic Synthesis
@en
Lewis Base Catalysis in Organic Synthesis
@nl
prefLabel
Lewis Base Catalysis in Organic Synthesis
@en
Lewis Base Catalysis in Organic Synthesis
@nl
P356
P1476
Lewis Base Catalysis in Organic Synthesis
@en
P2093
Gregory L. Beutner
Scott E. Denmark
P304
P356
10.1002/ANIE.200604943
P407
P577
2008-02-15T00:00:00Z