A formal [3,3]-sigmatropic rearrangement route to quaternary alpha-vinyl amino acids: use of allylic N-PMP trifluoroacetimidates.
about
Human serine racemase structure/activity relationship studies provide mechanistic insight and point to position 84 as a hot spot for β-elimination function.Use of Fluorinated Functionality in Enzyme Inhibitor Development: Mechanistic and Analytical AdvantagesAsymmetric synthesis of beta,gamma-unsaturated alpha-amino acids via efficient kinetic resolution with cinchona alkaloids.Synthesis and Deployment of an Elusive Fluorovinyl Cation Equivalent: Access to Quaternary α-(1'-Fluoro)vinyl Amino Acids as Potential PLP Enzyme Inactivators.Geometry-Retentive C-Alkenylation of Lithiated α-Aminonitriles: Quaternary α-Alkenyl Amino Acids and Hydantoins.
P2860
A formal [3,3]-sigmatropic rearrangement route to quaternary alpha-vinyl amino acids: use of allylic N-PMP trifluoroacetimidates.
description
2006 nî lūn-bûn
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年论文
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2006年论文
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name
A formal [3,3]-sigmatropic rea ...... c N-PMP trifluoroacetimidates.
@en
type
label
A formal [3,3]-sigmatropic rea ...... c N-PMP trifluoroacetimidates.
@en
prefLabel
A formal [3,3]-sigmatropic rea ...... c N-PMP trifluoroacetimidates.
@en
P2093
P2860
P356
P1433
P1476
A formal [3,3]-sigmatropic rea ...... c N-PMP trifluoroacetimidates.
@en
P2093
David B Berkowitz
P2860
P304
P356
10.1021/OL060019S
P407
P577
2006-03-01T00:00:00Z