A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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Solid-phase peptide synthesis (SPPS), C-terminal vs. side-chain anchoring: a reality or a myth.Copper(II)-mediated O-arylation of protected serines and threonines.Total synthesis of cyclic heptapeptide Rolloamide B.

P2860

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P2860

A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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http://www.wikidata.org/entity/Q58100778

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im August 2012 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

@nl

наукова стаття, опублікована в серпні 2012

@uk

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A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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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

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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

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

Synthetic and structural studies on syringolin A and B reveal critical determinants of selectivity and potency of proteasome inhibition

Automated mass spectrometric sequence determination of cyclic peptide library members.

Converting a peptide into a drug: strategies to improve stability and bioavailability.

Peptidomimetics and peptide backbone modifications.

Large-scale manufacture of peptide therapeutics by chemical synthesis.

Peptaibol antibiotics: a study on the helical structure of the 2-9 sequence of emerimicins III and IV.

Synthetic therapeutic peptides: science and market.

Chemical modifications designed to improve peptide stability: incorporation of non-natural amino acids, pseudo-peptide bonds, and cyclization.

N-terminal-prolonged vinyl ester-based peptides as selective proteasome beta1 subunit inhibitors.

New cyclic peptide proteasome inhibitors.

P304

11536-11540

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P31

scholarly article

P356

10.1002/CHEM.201201452

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

Pascal Verdié

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2012-08-02T00:00:00Z

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P698

22865765

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P921

general chemistry

A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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P2860

P2860

A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921