(Q52921616)

9 May 2018

title

Solid-phase peptide synthesis: from standard procedures to the synthesis of difficult sequences. (English)

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9 May 2018

author name string

Irene Coin

series ordinal

1

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9 May 2018

Michael Beyermann

series ordinal

2

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9 May 2018

Michael Bienert

series ordinal

3

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9 May 2018

publication date

1 January 2007

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9 May 2018

published in

Nature Protocols

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9 May 2018

volume

2

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9 May 2018

issue

12

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9 May 2018

page(s)

3247-3256

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9 May 2018

https://scigraph.springernature.com/pub.10.1038/nprot.2007.454

exact match

0 references

cites work

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Solid-phase peptide synthesis using mild base cleavage of N alpha-fluorenylmethyloxycarbonylamino acids, exemplified by a synthesis of dihydrosomatostatin

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Methods and protocols of modern solid phase Peptide synthesis

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The CRF peptide family and their receptors: yet more partners discovered

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Switch peptides in statu nascendi: induction of conformational transitions relevant to degenerative diseases.

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Synthesis of the nonacosapeptide corresponding to mammalian glucagon

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Structural analysis of WW domains and design of a WW prototype

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Use of N-tritylamino acids and PyAOP1 for the suppression of diketopiperazine formation in Fmoc/tBu solid-phase peptide synthesis using alkoxybenzyl ester anchoring linkages

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In situ neutralization in Boc-chemistry solid phase peptide synthesis. Rapid, high yield assembly of difficult sequences

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31 March 2020

Identifiers

DOI

10.1038/NPROT.2007.454

1 reference

9 May 2018

1 reference

9 May 2018