Dicyclopropylmethyl peptide backbone protectant. (Q33612577)

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6 February 2020

title

Dicyclopropylmethyl peptide backbone protectant (English)

1 reference

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6 February 2020

4

1 reference

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6 February 2020

author name string

Louis A Carpino

1

1 reference

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6 February 2020

Khaled Nasr

2

1 reference

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6 February 2020

Adel Ali Abdel-Maksoud

3

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6 February 2020

Dumitru Ionescu

5

1 reference

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6 February 2020

Peter Henklein

6

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6 February 2020

Holger Wenschuh

7

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6 February 2020

Michael Beyermann

8

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6 February 2020

Eberhard Krause

9

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6 February 2020

Michael Bienert

10

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6 February 2020

language of work or name

English

0 references

publication date

1 August 2009

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6 February 2020

1 reference

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6 February 2020

volume

11

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6 February 2020

issue

16

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6 February 2020

page(s)

3718-3721

1 reference

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Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

6 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

The aspartimide problem in Fmoc-based SPPS. Part III.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

The 'O-acyl isopeptide method' for the synthesis of difficult sequence-containing peptides: application to the synthesis of Alzheimer's disease-related amyloid beta peptide (Abeta) 1-42.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

The aspartimide problem in Fmoc-based SPPS. Part II.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

The aspartimide problem in Fmoc-based SPPS. Part I.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

The uronium/guanidinium Peptide coupling reagents: finally the true uronium salts

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811875

N,O‐bisFmoc derivatives of N‐(2‐hydroxy‐4‐methoxybenzyl)‐amino acids: Useful intermediates in peptide synthesis

30 October 2018

1 reference

12 December 2020

Incomplete Fmoc deprotection in solid-phase synthesis of peptides

1 reference

12 December 2020

Optimized preparation of deca(L-alanyl)-L-valinamide by 9-fluorenylmethyloxycarbonyl (Fmoc) solid-phase synthesis on polyethylene glycol-polystyrene (PEG-PS) graft supports, with 1,8-diazobicyclo [5.4.0]-undec-7-ene (DBU) deprotection

1 reference

12 December 2020

Pseudo-prolines (psi Pro) for accessing "inaccessible" peptides

1 reference

12 December 2020

Aminoacylpyrrolidine-2-nitriles: potent and stable inhibitors of dipeptidyl-peptidase IV (CD 26)

1 reference

12 December 2020

Identifiers

DOI

10.1021/OL901310Q

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19719204 AND SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

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6 February 2020

PubMed publication ID

19719204

1 reference