Trends to Acid-Labile Cys Protecting Groups: Thp as an Efficient and Non-Aromatic Cys Protecting Group for Fmoc Chemistry (original) (raw)

Side reactions in the SPPS of Cys-containing peptides

Amino Acids, 2013

Use of the Npys thiol protection in solid phase peptide synthesis Application to direct peptide-protein conjugation through cysteine residues

David Andreu

International Journal of Peptide and Protein Research, 1989

View PDFchevron_right

Fundamentals of Modern Peptide Synthesis

Jean-alain Fehrentz

ChemInform, 2006

View PDFchevron_right

Specific chemical cleavage in high yield at the amino peptide bonds of cysteine and cystine residues. J. Biol. Chem. 248, 6583-6591

Thomas Vanaman

Journal of Biological Chemistry

View PDFchevron_right

Chemical Cleavage of an Asp-Cys Sequence Allows Efficient Production of Recombinant Peptides with an N-Terminal Cysteine Residue

Katia Pane

Bioconjugate chemistry, 2018

View PDFchevron_right

Chemical Ligation of S-Scylated Cysteine Peptides to Form Native Peptides via 5-, 11-, and 14-Membered Cyclic Transition States ‡

Keyur Pandya

The Journal of Organic Chemistry, 2011

View PDFchevron_right

Practical protocols for stepwise solid-phase synthesis of cysteine-containing peptides

Yvonne Angell

Journal of Peptide Research, 2002

View PDFchevron_right

Synthesis of N α-(1-Phenyl-2-mercaptoethyl) Amino Acids, New Building Blocks for Ligation and Cyclization at Non-Cysteine Sites: Scope and Limitations in Peptide …

Paolo Botti

The Journal of Organic …, 2004

View PDFchevron_right

Synthesis of N α -(1-Phenyl-2-mercaptoethyl) Amino Acids, New Building Blocks for Ligation and Cyclization at Non-Cysteine Sites: Scope and Limitations in Peptide Synthesis

Paolo Botti

The Journal of Organic Chemistry, 2004

View PDFchevron_right

Side reaction withN-carboxymethyl amino acids in the synthesis of backbone cyclized peptides

Diana Imhof

Letters in Peptide Science, 1998

View PDFchevron_right

Solvent-Free Synthesis of Bhc-Cl and Application to Cysteine Protection in Solid Phase Peptide Synthesis

Jane Wissinger

Peptides Across the Pacific: The Proceedings of the Twenty-Third American and the Sixth International Peptide Symposium, 2013

View PDFchevron_right

Application of dimethylsulphoxide(DMSO) / trifluoroacetic acid(TFA) oxidation to the synthesis of cystine-containing peptide

Ahmed Shide

Tetrahedron Letters, 1991

View PDFchevron_right

Peptide synth

Shivaramakrishnan Kumar

View PDFchevron_right

Peptides: Chemistry, structure and biology

Pravin Kaumaya

FEBS Letters, 1977

View PDFchevron_right

S-2,4,6-trimethoxybenzyl (Tmob): a novel cysteine protecting group for the N.alpha.-(9-fluorenylmethoxycarbonyl) (Fmoc) strategy of peptide synthesis

George Barany

The Journal of Organic Chemistry, 1992

View PDFchevron_right

Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis

Hortensia Maria Rodriguez Cabrera

ChemistryOpen, 2017

View PDFchevron_right

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

Dimitrios Gatos

International Journal of Peptide and Protein Research, 1996

View PDFchevron_right

ChemInform Abstract: Building Units for N-Backbone Cyclic Peptides. Part 1. Synthesis of Protected N-(ω-Aminoalkylene)amino Acids and Their Incorporation into Dipeptide Units

Chaim Gilon

ChemInform, 1993

View PDFchevron_right

Tetrahydropyranyl, a Nonaromatic Acid-Labile Cys Protecting Group for Fmoc Peptide Chemistry

Iván Ramos-Tomillero, Hortensia Rodriguez

View PDFchevron_right

Building units for N-backbone cyclic peptides. Part 4.1 Synthesis of protected Nα-functionalized alkyl amino acids by reductive alkylation of natural amino acids

Ron Kasher, Chaim Gilon, Evgenia Glukhov

Journal of the Chemical Society, Perkin Transactions 1, 1997

View PDFchevron_right

Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and estersviacomplimentary strategies

Jennifer Stockdill

Chemical Science, 2018

View PDFchevron_right

Side-chain anchoring strategy for solid-phase synthesis of peptide acids with C-terminal cysteine

George Barany

Biopolymers, 2003

View PDFchevron_right

Extending the Scope of Native Chemical Peptide Coupling

Christian Haase

Angewandte Chemie International Edition, 2008

View PDFchevron_right

Introductory Chapter: Peptide Synthesis

jaya varkey

Peptide Synthesis, 2019

View PDFchevron_right

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

View PDFchevron_right

Boc-S-methylbenzyl-(S)-2-amino-6-mercaptohexanoic acid: Preparation and application to the synthesis of a large cyclic disulfide peptide

Julio Camarero

Tetrahedron Letters, 1995

View PDFchevron_right

Methylthiomethyl, a new carboxyl protecting group in peptide synthesis

Arnaldo Dossena

International journal of peptide and protein research, 1984

View PDFchevron_right

Cyclic peptides from unprotected precursors through ring-chain tautomerism

Paolo Botti

Chinese Peptide Symposia, 2002

View PDFchevron_right

New methods for the synthesis of biologically active cyclic peptides

Varsha Thombare

2019

View PDFchevron_right

The chemistry of Amino Acid and Peptides via Solution-Phase-Peptide Synthesis

Gaber Osman

Egyptian Journal of Chemistry, 2021

View PDFchevron_right

Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditions

N. Thieriet

Tetrahedron Letters, 1997

View PDFchevron_right

Recent development of peptide coupling reagents in organic synthesis

Ayman El-Faham

Tetrahedron, 2004

View PDFchevron_right

Trends to Acid-Labile Cys Protecting Groups: Thp as an Efficient and Non-Aromatic Cys Protecting Group for Fmoc Chemistry (original) (raw)

Related papers