A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

about

Unexpected hydrolytic instability of N-acylated amino acid amides and peptides.Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations.A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

P2860

Q37701583-4F5A0CAC-6947-4406-9B51-B70B87B75F4C Q51429455-7D0BAEFE-EB3F-4BE6-A83F-ED3E63533D97 Q58100778-9A28304A-981F-464A-8EFF-6BB7186F90E8

P2860

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

Item

http://www.wikidata.org/entity/Q46506350

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

2010年學術文章

@zh-hant

name

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@en

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@nl

type

Item

label

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@en

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@nl

prefLabel

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@en

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@nl

P1476

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

@en

P2093

Gaël Nomezine

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

Gilles Subra

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

Maciej Pawłowski

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

Muriel Amblard

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

Nicolas Masurier

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

Paweł Zajdel

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

P2860

Structure-activity relationships of the melanocortin tetrapeptide Ac-His-DPhe-Arg-Trp-NH(2) at the mouse melanocortin receptors: part 2 modifications at the Phe position.

A new class of arylpiperazine derivatives: the library synthesis on SynPhase lanterns and biological evaluation on serotonin 5-HT(1A) and 5-HT(2A) receptors.

Methods and protocols of modern solid phase Peptide synthesis.

Construction of protein analogues by site-specific condensation of unprotected fragments.

Solid-phase synthesis of FKBP12 inhibitors: N-sulfonyl and N-carbamoylprolyl/pipecolyl amides.

Solid-phase synthesis of arginine-containing peptides and fluorogenic substrates using a side-chain anchoring approach.

Analogues of AVP modified in the N-terminal part of the molecule with Pip isomers: TFA-catalysed peptide bond hydrolysis.

Mechanistic studies of amide bond scission during acidolytic deprotection of Pip containing peptide.

Backbone Amide Linker (BAL) Strategy forNα-9-Fluorenylmethoxycarbonyl (Fmoc) Solid-Phase Synthesis of Unprotected Peptidep-Nitroanilides and Thioesters1

Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides1,2,3

P304

7547-7553

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

P31

scholarly article

P356

10.1002/CHEM.201000313

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

P407

English

P433

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

P478

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

P50

Jean Martinez

P577

2010-07-01T00:00:00Z

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

P698

20468039

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

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

about

P2860

P2860

A new highly versatile handle for chemistry on a solid support: the pipecolic linker.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698