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aspartimide
Known as:
2,5-Pyrrolidinedione, 3-amino-
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Aspartic Acid
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Aspartimide modified galanin analogue antagonizes galanin action on insulin secretion.
J. Ruczyński
,
Z. Konstański
,
M. Cybal
,
I. Kocić
,
P. Rekowski
Protein Peptide Letters
2010
Corpus ID: 23109058
Aspartimide (Asi) formation is one of the most serious side reactions that can occur both during solid phase synthesis and…
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2010
2010
Synthesis of N-linked glycopeptides via solid-phase aspartylation.
Trent Conroy
,
K. Jolliffe
,
R. Payne
Organic and biomolecular chemistry
2010
Corpus ID: 22526185
An efficient strategy for the preparation of N-linked glycopeptides is described. The method relies on the use of side chain…
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2009
2009
Design of protecting groups for the beta-carboxylic group of aspartic acid that minimize base-catalyzed aspartimide formation.
A. Karlström
,
A. Undén
International journal of peptide & protein…
2009
Corpus ID: 25257550
With the objectives of developing new protecting groups for the beta-carboxyl group of aspartic acid that are resistant to base…
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2008
2008
Problem of aspartimide formation in Fmoc‐based solid‐phase peptide synthesis using Dmab group to protect side chain of aspartic acid
J. Ruczyński
,
B. Lewandowska
,
P. Mucha
,
P. Rekowski
Journal of Peptide Science
2008
Corpus ID: 46256037
The sequence‐dependent, acid‐ or base‐catalysed aspartimide formation is one of the most serious side reactions in solid‐phase…
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2008
2008
Synthesis and Characterization of a POSS-Maleimide Precursor for Hybrid Nanocomposites
Seetharaman Jothibasu
,
S. Premkumar
,
M. Alagar
,
I. Hamerton
2008
Corpus ID: 93484221
Epoxy polyhedral oligomeric silsesquioxane (POSS)-based hybrid nanocomposites were prepared by in situ polymerization of a…
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2005
2005
α‐ and β‐ aspartyl peptide ester formation via aspartimide ring opening
P. Stathopoulos
,
Serafim Papas
,
S. Kostidis
,
V. Tsikaris
Journal of Peptide Science
2005
Corpus ID: 24791690
The undesirable reaction of aspartimide formation has been proved to occur under both acid and base conditions in solid‐phase…
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2003
2003
Synthesis of peptide sequences related to thrombospondin: factors affecting aspartimide by-product formation.
J. Cebrian
,
V. Domingo
,
F. Reig
Journal of Peptide Research
2003
Corpus ID: 39595748
Aspartimide formation is one of the most common secondary reactions on solid phase peptide synthesis. In the present work, we…
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Highly Cited
2000
Highly Cited
2000
Peptide thioester preparation by Fmoc solid phase peptide synthesis for use in native chemical ligation
A. Clippingdale
,
C. Barrow
,
J. Wade
Journal of Peptide Science
2000
Corpus ID: 24465330
Established methodology for the preparation of peptide thioesters requires the use of t‐butoxycarbonyl chemistry owing to the…
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1996
1996
Solid-phase synthesis of tailed cyclic peptides: The use of α-allyl-protected aspartic acid leads to aspartimide and tetramethylguanidinium formation
D. Delforge
,
M. Dieu
,
+6 authors
J. Remacle
Letters in peptide science
1996
Corpus ID: 21264131
This paper discusses the application of a method developed for cyclic peptide synthesis using allyl-based sidechain-protecting…
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Highly Cited
1988
Highly Cited
1988
Mechanisms of aspartimide formation: the effects of protecting groups, acid, base, temperature and time.
J. Tam
,
M. W. Riemen
,
R. B. Merrifield
Peptide research
1988
Corpus ID: 20845623
Factors affecting aspartimide formation, such as protecting groups, acidity, basicity, and temperature, were studied using the…
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