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Building Bridges: Biocatalytic C–C-Bond Formation toward Multifunctional ProductsMechanistic investigation of the enantioselective intramolecular stetter reaction: proton transfer is the first irreversible stepQuantum mechanical investigation of the effect of catalyst fluorination in the intermolecular asymmetric Stetter reaction.Catalytic asymmetric intermolecular Stetter reactions of enolizable aldehydes with nitrostyrenes: computational study provides insight into the success of the catalyst.Novel carbon-carbon bond formations for biocatalysis.Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products.The Enzymology of Organic Transformations: A Survey of Name Reactions in Biological Systems.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.Catalytic asymmetric intermolecular Stetter reaction of enals with nitroalkenes: enhancement of catalytic efficiency through bifunctional additives.Asymmetric Stetter reactions catalyzed by thiamine diphosphate-dependent enzymes.Enzymatic Chemoselective Aldehyde-Ketone Cross-Couplings through the Polarity Reversal of Methylacetoin.Highly Enantioselective Intermolecular Stetter Reaction of Simple Acrylates: Synthesis of α-Chiral γ-KetoestersHighly Asymmetric NHC-Catalyzed Hydroacylation of Unactivated AlkenesHoch enantioselektive Synthese von α-Aminosäurederivaten durch NHC-katalysierte intermolekulare Stetter-ReaktionBiocatalytic Enantioselective Oxidative CC Coupling by Aerobic CH ActivationBiocatalytic Oxidative CC Bond Formation Catalysed by the Berberine Bridge Enzyme: Optimal Reaction Conditions
P2860
Q26741385-BE1D2369-18A1-4043-A5B0-52AE29E4755FQ34722960-BCD32102-554B-4BC9-9DDD-8AAB1F34077FQ35126822-00285F35-4B1B-4D30-A757-278B66E42899Q35956101-1205EE8E-3CE5-4D82-A39E-5DD4F7C20E6DQ37847523-9AE83927-AF10-4AB0-B89D-E39098F91863Q38868210-D964DA70-A548-4F7E-8FDC-6804227D7FC2Q38922927-2E57E006-7577-48A4-98DA-B32E9EA7E51AQ39240715-5201FBDC-5827-4FE3-8627-7C61D9501481Q42230701-7D49A22A-D9BC-4D9C-B5F4-8418564D1DDEQ46875471-41C5E725-2585-4704-AF8E-C404508BD250Q54269727-E56060F5-A0EA-4BB1-B56A-EE9E8600DCD5Q57657259-AD68AEEA-BC4D-4CC4-987F-6ADBBB21D52FQ57657320-C5B109D9-C3AB-493D-9099-7E845662BFD5Q57657324-0191B34A-BDC8-46D8-AE31-DF7F41098A7DQ57978257-32439F82-B4F9-40F2-A05C-BB0E34FC08D9Q57978260-A3660D3C-8154-4501-AB2B-929F102C60B1
P2860
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
The enzymatic asymmetric conjugate umpolung reaction.
@en
The enzymatic asymmetric conjugate umpolung reaction.
@nl
type
label
The enzymatic asymmetric conjugate umpolung reaction.
@en
The enzymatic asymmetric conjugate umpolung reaction.
@nl
prefLabel
The enzymatic asymmetric conjugate umpolung reaction.
@en
The enzymatic asymmetric conjugate umpolung reaction.
@nl
P2093
P356
P1476
The enzymatic asymmetric conjugate umpolung reaction.
@en
P2093
Carola Dresen
Martina Pohl
Michael Müller
Michael Richter
P304
P356
10.1002/ANIE.201000632
P407
P577
2010-09-01T00:00:00Z