Advances in Fmoc solid‐phase peptide synthesis - Behrendt - 2016 - Journal of Peptide Science - Wiley Online Library
PEPTIDE SYNTHESIS
An important side reaction using the thiol, 3,6‐dioxa‐1,8‐octanedithiol (DODT), in 9‐fluorenylmethoxycarbonyl‐based solid phase peptide synthesis - Harris - 2014 - Journal of Peptide Science - Wiley Online Library
Methods and Protocols
MIAMI UNIVERSITY
PEPTIDE SYNTHESIS
Solid-Phase Peptide Synthesis of Dipeptide (Histidine-β-Alanine) as a Chelating Agent by Using Trityl Chloride Resin, for Removal of Al3+, Cu2+, Hg2+ and Pb2+: Experimental and Theoretical Study
Solid-Phase Peptide Synthesis of Dipeptide (Histidine-β-Alanine) as a Chelating Agent by Using Trityl Chloride Resin, for Removal of Al3+, Cu2+, Hg2+ and Pb2+: Experimental and Theoretical Study
PDF) Peptide synthesis: Chemical or enzymatic
Contents:
An important side reaction using the thiol, 3,6â•'dioxaâ•'1,8â•'octanedithiol (DODT), in 9â•'fluorenylmethox
Reductions with hydrosilanes - Wikipedia
PDF) 1,4-Benzenedimethanethiol (1,4-BDMT) as a scavenger for greener peptide resin cleavages
Solid-Phase Peptide Synthesis | SpringerLink
Methods and Protocols
The chemistry and biology of guanidine secondary metabolites - Natural Product Reports (RSC Publishing) DOI:10.1039/D0NP00051E
1,4-Benzenedimethanethiol (1,4-BDMT) as a scavenger for greener peptide resin cleavages - RSC Advances (RSC Publishing)
CSIRO PUBLISHING | Australian Journal of Chemistry
WO2014033466A1 - Method and compositions for removing acid-labile protecting groups - Google Patents
The synthesis and reactivity of optically pure amino acids bearing side-chain thioamides - Journal of the Chemical Society, Perkin Transactions 1 (RSC Publishing) DOI:10.1039/B004688O
PEPTIDE SYNTHESIS
PEPTIDE SYNTHESIS
Reduction of cysteine-S-protecting groups by triisopropylsilane. - Abstract - Europe PMC
Peptidomimetics: Fmoc Solid-Phase Pseudopeptide Synthesis | SpringerLink
