(Q43588287)

24 November 2017

title

Acid-labile protecting groups for the synthesis of lipidated peptides (English)

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24 November 2017

4

Waldmann H

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24 November 2017

Kadereit D

1

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24 November 2017

Deck P

series ordinal

2

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24 November 2017

Heinemann I

series ordinal

3

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24 November 2017

language of work or name

English

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publication date

1 March 2001

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Chemistry—A European Journal

24 November 2017

published in

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24 November 2017

volume

7

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24 November 2017

issue

6

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24 November 2017

page(s)

1184-1193

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Bioorganic synthesis of lipid-modified proteins for the study of signal transduction.

24 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Extremely mild reagent for Boc deprotection applicable to the synthesis of peptides with thioamide linkages

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Organic Synthesis and Biological Signal Transduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Synthesis of the N-Terminal N-Myristoylated and S-Palmitoylated Undetrigintapeptide of Endothelial NO-Synthase This research was supported by the Fonds der Chemischen Industrie and the Deutsche Forschungsgemeinschaft

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Solution phase synthesis of Saccharomyces cerevisiae a-mating factor and its analogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Preparation of the very acid‐sensitive Fmoc‐Lys(Mtt)‐OH Application in the synthesis of side‐chain to side‐chain cyclic peptides and oligolysine cores suitable for the solid‐phase assembly of MAPs and TASPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Synthesis of characteristic H-Ras lipopeptides by employing noble-metal-, acid-, and reduction-labile blocking groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

Synthesis of the very acid-sensitive Fmoc-Cys(Mmt)-OH and its application in solid-phase peptide synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010316%297%3A6%3C1184%3A%3AAID-CHEM1184%3E3.0.CO%3B2-5

10.1002/1521-3765(20010316)7:6<1184::AID-CHEM1184>3.0.CO;2-5

21 January 2018

Identifiers

DOI

1 reference

24 November 2017

1 reference