Chemoenzymatic synthesis of all four diastereomers of 2,6-disubstituted piperidines through stereoselective monoamination of 1,5-diketones.
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Characterization of a recombinant (+)-γ-lactamase from Microbacterium hydrocarbonoxydans which provides evidence that two enantiocomplementary γ-lactamases are in the strain.Artificial concurrent catalytic processes involving enzymes.Cascade catalysis--strategies and challenges en route to preparative synthetic biology.The Industrial Age of Biocatalytic Transamination.Concise Chemoenzymatic Three Step Total Synthesis of Isosolenopsin Through Medium Engineering.The role of biocatalysis in the asymmetric synthesis of alkaloids.Asymmetric Preparation of prim-, sec-, and tert-Amines Employing Selected Biocatalysts.Beyond Chemoselectivity: Catalytic Site-Selective Aldolization of Diketones and Exploitation for Enantioselective Alzheimer's Drug Candidate Synthesis.
P2860
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P2860
Chemoenzymatic synthesis of all four diastereomers of 2,6-disubstituted piperidines through stereoselective monoamination of 1,5-diketones.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@en
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@nl
type
label
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@en
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@nl
prefLabel
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@en
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@nl
P2860
P356
P1476
Chemoenzymatic synthesis of al ...... onoamination of 1,5-diketones.
@en
P2093
Ferdinand Zepeck
Robert C Simon
P2860
P304
P356
10.1002/CHEM.201202793
P407
P577
2013-01-04T00:00:00Z