Deprotection Strategies for Thioimidates During Fmoc Solid-Phase Peptide Synthesis: A Safe Route to Thioamides

doi 10.26434/chemrxiv.9700118
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Chemical Society (ACS)

Related search

Boosting Fmoc Solid-Phase Peptide Synthesis by Ultrasonication

English

Facile Synthesis of Internal and C-Terminal Peptide Α -Ketoamides With Fmoc-Solid Phase Peptide Synthesis

Helvetica Chimica Acta
Organic ChemistryTheoretical ChemistryBiochemistryInorganic ChemistryDrug DiscoveryCatalysisPhysical
2018English

Fmoc Solid-Phase Peptide Synthesis of Human Alfa-Calcitonin Gene-Related Peptide and Two Fluorescent Analogs

2015English

Studies on Peptides. CLXV. Combination of a New Amide-Precursor Reagent and Trimethylsilyl Bromide Deprotection for the 9-Fluorenylmethyloxycarbonyl-Based Solid-Phase Synthesis of Chicken Antral Peptide.

Chemical and Pharmaceutical Bulletin
MedicineDrug DiscoveryChemistry
1988English

Peptide Synthesis in Water IV. Preparation of N-Ethanesulfonylethoxycarbonyl (Esc) Amino Acids and Their Application to Solid Phase Peptide Synthesis

Chemical and Pharmaceutical Bulletin
MedicineDrug DiscoveryChemistry
2004English

Covalent Epitope Decoration of Carbon Electrodes Using Solid Phase Peptide Synthesis

Scientific Reports
Multidisciplinary
2019English

Solid-Phase Synthesis of Aza-Lysine Peptide Analogue of Trypsin Substrate

2015English

A Rapid Deprotection Procedure for Phosphotriester DNA Synthesis

Nucleosides and Nucleotides
1985English

Solid-Phase Synthesis of a Special Phosphorylated Peptide as a Biomarker for LC–MS/MS Detection for OPNA Exposure

Synlett
Organic Chemistry
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy