Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine.

about

Perfluoroalkylation of Alkenes by Frustrated Lewis Pairs.Position-dependent impact of hexafluoroleucine and trifluoroisoleucine on protease digestion.Fluorinated amino acids in amyloid formation: a symphony of size, hydrophobicity and α-helix propensity

P2860

Q48281497-F38FDAEE-F94B-4DE1-89F2-93220735E213 Q52725083-9AFEB37F-1984-41A1-9D8D-E867731C252E Q57528330-BA47B866-A795-464E-BDF7-D0F28156BD44

P2860

Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine.

Item

http://www.wikidata.org/entity/Q41969605

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Synthesis of enantiomerically ...... 5,5-trifluoro-allo-isoleucine.

@en

type

Item

label

Synthesis of enantiomerically ...... 5,5-trifluoro-allo-isoleucine.

@en

prefLabel

Synthesis of enantiomerically ...... 5,5-trifluoro-allo-isoleucine.

@en

P1476

Synthesis of enantiomerically ...... 5,5-trifluoro-allo-isoleucine.

@en

P2093

Constantin Czekelius

http://www.w3.org/2001/XMLSchema#string

Dieter Lentz

http://www.w3.org/2001/XMLSchema#string

Elisabeth K Nyakatura

http://www.w3.org/2001/XMLSchema#string

Holger Erdbrink

http://www.w3.org/2001/XMLSchema#string

Ulla I M Gerling

http://www.w3.org/2001/XMLSchema#string

P2860

Structural basis for the enhanced stability of highly fluorinated proteins

Modulating protein structure with fluorous amino acids: increased stability and native-like structure conferred on a 4-helix bundle protein by hexafluoroleucine.

Stabilization of bzip peptides through incorporation of fluorinated aliphatic residues.

Molecular dynamics guided study of salt bridge length dependence in both fluorinated and non-fluorinated parallel dimeric coiled-coils.

A coiled coil with a fluorous core.

Incorporation of trifluoroisoleucine into proteins in vivo.

Towards identifying preferred interaction partners of fluorinated amino acids within the hydrophobic environment of a dimeric coiled coil peptide.

The design of coiled-coil structures and assemblies.

Determination of intrinsic hydrophilicity/hydrophobicity of amino acid side chains in peptides in the absence of nearest-neighbor or conformational effects.

Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids.

P304

2009-2014

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3762/BJOC.9.236

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Beate Koksch

Susanne Huhmann

P577

2013-10-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

258350509

http://www.w3.org/2001/XMLSchema#string

P698

24204411

http://www.w3.org/2001/XMLSchema#string

P932

3817528

http://www.w3.org/2001/XMLSchema#string

Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine.

about

P2860

P2860

Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P932