Induced axial chirality in the biphenyl core of the proatropoisomeric, C alpha-tetrasubstituted alpha-amino acid residue Bip in peptides.
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Recent Progress on the Stereoselective Synthesis of Cyclic Quaternary alpha-Amino Acids.Chirality sensing using stereodynamic probes with distinct electronic circular dichroism output.Substrate-Specific Amino Acid Sensing Using a Molecular d/ l-Cysteine Probe for Comprehensive Stereochemical Analysis in Aqueous Solution.Helical screw-sense preferences of peptides based on chiral, Cα-tetrasubstituted α-amino acids.
P2860
Induced axial chirality in the biphenyl core of the proatropoisomeric, C alpha-tetrasubstituted alpha-amino acid residue Bip in peptides.
description
2005 nî lūn-bûn
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name
Induced axial chirality in the ...... acid residue Bip in peptides.
@en
Induced axial chirality in the ...... acid residue Bip in peptides.
@nl
type
label
Induced axial chirality in the ...... acid residue Bip in peptides.
@en
Induced axial chirality in the ...... acid residue Bip in peptides.
@nl
prefLabel
Induced axial chirality in the ...... acid residue Bip in peptides.
@en
Induced axial chirality in the ...... acid residue Bip in peptides.
@nl
P2093
P50
P356
P1476
Induced axial chirality in the ...... o acid residue Bip in peptides
@en
P2093
Anne Gaucher
Bernard Kaptein
Fernando Formaggio
Jean-Paul Mazaleyrat
Karen Wright
Laurence Dutot
Michel Wakselman
Nathalie Toulemonde
Quirinus B Broxterman
P304
P356
10.1002/CHEM.200500187
P407
P577
2005-11-01T00:00:00Z