A backbone amide protecting group for overcoming difficult sequences and suppressing aspartimide formation

about

Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation.Adapting the Glaser Reaction for Bioconjugation: Robust Access to Structurally Simple, Rigid Linkers.

P2860

Q47353754-2E3C582E-1561-48D8-88BF-41CFA6A51D55 Q48161924-B83336E9-EF33-45F3-8E02-7BA27626806D

P2860

A backbone amide protecting group for overcoming difficult sequences and suppressing aspartimide formation

Item

http://www.wikidata.org/entity/Q41531093

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

A backbone amide protecting gr ...... pressing aspartimide formation

@en

type

Item

label

A backbone amide protecting gr ...... pressing aspartimide formation

@en

prefLabel

A backbone amide protecting gr ...... pressing aspartimide formation

@en

P1476

A backbone amide protecting gr ...... pressing aspartimide formation

@en

P2093

George Papageorgiou

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

Martin Quibell

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

Richard Raz

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

P2860

Analysis of peptides and proteins containing nitrotyrosine by matrix-assisted laser desorption/ionization mass spectrometry.

Automated synthesis of backbone protected peptides.

Enhancement of solubility by temporary dimethoxybenzyl-substitution of peptide bonds. Towards the synthesis of defined oligomers of alanine and of lysyl-glutamyl-glycine.

Chemical synthesis of peptides and proteins.

Chemical synthesis of ubiquitin, ubiquitin-based probes, and diubiquitin

Ion-spray tandem mass spectrometry in peptide synthesis: structural characterization of minor by-products in the synthesis of ACP(65-74).

Expediting the Fmoc solid phase synthesis of long peptides through the application of dimethyloxazolidine dipeptides.

Mass spectrometric evaluation of synthetic peptides for deletions and insertions.

New t-butyl based aspartate protecting groups preventing aspartimide formation in Fmoc SPPS.

An activated O --> N acyl transfer auxiliary: efficient amide-backbone substitution of hindered "difficult" peptides.

P304

360-367

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

P31

scholarly article

P356

10.1002/PSC.2877

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

P433

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

P478

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

P50

Fabienne Burlina

John Offer

Abu-Baker M Abdel-Aal

P577

2016-04-18T00:00:00Z

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

P698

27086749

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

P932

5074248

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

A backbone amide protecting group for overcoming difficult sequences and suppressing aspartimide formation

about

P2860

P2860

A backbone amide protecting group for overcoming difficult sequences and suppressing aspartimide formation

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932