Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions

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Advances in Fmoc solid-phase peptide synthesis A copper-catalyzed reaction of oximes with diisopropyl azodicarboxylate: an alternative method for the synthesis of oxime carbonates.K-Oxyma: a Strong Acylation-Promoting, 2-CTC Resin-Friendly Coupling Additive

P2860

Q26770921-12F49695-13B7-4768-8751-5C0FA3603165 Q48351054-08C7B28A-927B-45EE-84A4-1963450D5978 Q58035051-8413A762-E692-4FA1-91BC-E05F948170C8

P2860

Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions

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http://www.wikidata.org/entity/Q58035166

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im Mai 2010 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

@nl

наукова стаття, опублікована в травні 2010

@uk

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Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@en

Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@nl

type

Item

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Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@en

Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@nl

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Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@en

Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@nl

P1476

Oxime Carbonates: Novel Reagen ...... Groups, Free of Side Reactions

@en

P2093

Ayman El-Faham

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

Fernando Albericio

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

Ramon Subirós-Funosas

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

Sherine N. Khattab

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

P2860

Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonates

9-Fluorenylmethoxycarbonyl amino-protecting group

COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents.

Orthogonal protecting groups for N(alpha)-amino and C-terminal carboxyl functions in solid-phase peptide synthesis.

Amino acid-protecting groups.

Identification of Fmoc-beta-Ala-OH and Fmoc-beta-Ala-amino acid-OH as new impurities in Fmoc-protected amino acid derivatives.

Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion.

Convergent approaches for the synthesis of the antitumoral peptide, Kahalalide F. Study of orthogonal protecting groups.

Fmoc-2-mercaptobenzothiazole, for the introduction of the Fmoc moiety free of side-reactions.

Microwave irradiation and COMU: a potent combination for solid-phase peptide synthesis

P304

3275-3280

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

P31

scholarly article

P356

10.1002/EJOC.201000028

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

P433

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

P478

2010

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

P577

2010-05-04T00:00:00Z

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

Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions

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P2860

P2860

Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577