Inverting the regioselectivity of the berberine bridge enzyme by employing customized fluorine-containing substrates.
about
Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.Deracemization by simultaneous bio-oxidative kinetic resolution and stereoinversion.Facile total synthesis of lysicamine and the anticancer activities of the RuII, RhIII, MnII and ZnII complexes of lysicamineControlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4-tetrahydroisoquinoline derivatives.The role of biocatalysis in the asymmetric synthesis of alkaloids.Asymmetric Preparation of prim-, sec-, and tert-Amines Employing Selected Biocatalysts.Deracemisation of benzylisoquinoline alkaloids employing monoamine oxidase variants
P2860
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P2860
Inverting the regioselectivity of the berberine bridge enzyme by employing customized fluorine-containing substrates.
description
2012 nî lūn-bûn
@nan
2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
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name
Inverting the regioselectivity ...... luorine-containing substrates.
@en
Inverting the regioselectivity ...... luorine-containing substrates.
@nl
type
label
Inverting the regioselectivity ...... luorine-containing substrates.
@en
Inverting the regioselectivity ...... luorine-containing substrates.
@nl
prefLabel
Inverting the regioselectivity ...... luorine-containing substrates.
@en
Inverting the regioselectivity ...... luorine-containing substrates.
@nl
P2860
P50
P356
P1476
Inverting the regioselectivity ...... luorine-containing substrates.
@en
P2093
Silvia Wallner
Verena Resch
P2860
P304
13173-13179
P356
10.1002/CHEM.201201895
P407
P577
2012-09-07T00:00:00Z