A Novel Protecting/Activating Strategy for β-Hydroxy Acids and Its Use in Convergent Peptide Synthesis † (original) (raw)
Synthesis and application of acid labile anchor groups for the synthesis of peptide amides by Fmoc-solid-phase peptide synthesis
Jochen Knolle
International journal of peptide and protein research, 1989
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Journal of Combinatorial Chemistry, 2000
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George Barany
The Journal of Organic Chemistry, 1996
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Facile solid-phase synthesis of C-terminal peptide aldehydes and hydroxamates from a common Backbone Amide-Linked (BAL) intermediate*†
Sharon Gazal, Larry R . Masterson
The Journal of Peptide Research, 2008
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Application of N-(tert-butyloxycarbonyl)amino acid N-carboxyanhydrides in solid-phase peptide synthesis
Fred Naider
The Journal of Organic Chemistry, 1993
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Facile solid-phase synthesis of C-terminal peptide aldehydes and hydroxamates from a common Backbone Amide-Linked (BAL) intermediate*†: Synthesis of peptide aldehydes and hydroxamates
Larry R . Masterson
Journal of Peptide Research, 2008
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Synthesis of 5-(((R,S)-5-((9-Fluorenylmethoxycarbonyl)amino)-10,11-dihydrodibenzo[a,d]cyclohepten-2-yl)oxy)valeric Acid (CHA) and 5-(((R,S)-5-((9-Fluorenylmethoxycarbonyl)amino)dibenzo[a,d]-cyclohepten-2-yl)oxy)valeric Acid (CHE) Handles for the Solid-Phase Synthesis of C-Terminal Peptide Amides ...
Kiyoshi Nokihara
The Journal of Organic Chemistry, 1994
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Jean-alain Fehrentz
ChemInform, 2006
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Ferenc Hudecz
Tetrahedron, 1998
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Francesc Rabanal
Tetrahedron Letters, 1992
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Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis
Hortensia Maria Rodriguez Cabrera
ChemistryOpen, 2017
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Direct cleavage of peptides from a solid support into aqueous buffer. Application in simultaneous multiple peptide synthesis
Rhonda Campbell
The Journal of Organic Chemistry, 1991
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Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides1,2,3
George Barany
Journal of the American Chemical Society, 1998
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Green Solvent Mixtures for Solid-Phase Peptide Synthesis: A Dimethylformamide-Free Highly Efficient Synthesis of Pharmaceutical-Grade Peptides
Walter Cabri
ACS Sustainable Chemistry & Engineering, 2019
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Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides 1 , 2 , 3
Josef Vagner
Journal of the American Chemical Society, 1998
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Sascha Knauer
2020
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4-Alkoxy-2-hydroxybenzaldehyde (AHB): A Versatile Aldehyde Linker for Solid-Phase Synthesis of C-Terminal Modified Peptides and Peptidomimetics †
Victor Hruby
Organic Letters, 2000
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Ferenc Fülöp
Organic Letters, 2004
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Predrag Cudic
Amino Acids, 2013
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Ramon Eritja
Tetrahedron Letters, 1992
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Piotr Wieczorek
Liebigs Annalen der Chemie, 1988
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Ramon Eritja
Cheminform, 1993
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Diana Imhof
Journal of Peptide Research, 1999
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Acetophenone-based linker for solid-phase peptide synthesis
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Journal of Peptide Science, 2000
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Selective deprotection of the N.alpha.-tert-butyloxycarbonyl group in solid phase peptide synthesis with chlorotrimethylsilane in phenol
Francis Picart
Journal of Organic Chemistry, 1993
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The synthesis of ‘difficult’ peptides using 2-hydroxy-4-methoxybenzyl or pseudoproline amino acid building blocks: a comparative study
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Journal of Peptide Science, 1999
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High Throughput Synthesis of Peptides and Peptidomimetics
Victor Hruby is to
ChemInform, 2007
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