![SOLVED: Fmoc-Cl is a common protecting group for amino acids. What other problem might arise with this amino acid during peptide synthesis? SOLVED: Fmoc-Cl is a common protecting group for amino acids. What other problem might arise with this amino acid during peptide synthesis?](https://cdn.numerade.com/ask_images/aa2bcc6dc0c24744b23a4e95e1e73a0c.jpg)
SOLVED: Fmoc-Cl is a common protecting group for amino acids. What other problem might arise with this amino acid during peptide synthesis?
![An Efficient Synthesis of Nα-Protected Amino and Peptide Acid Aryl Amides via Iodine-Mediated Oxidative Acylation of Nα-Protected Amino and Peptide Thioacids An Efficient Synthesis of Nα-Protected Amino and Peptide Acid Aryl Amides via Iodine-Mediated Oxidative Acylation of Nα-Protected Amino and Peptide Thioacids](https://www.organic-chemistry.org/abstracts/lit4/200m.gif)
An Efficient Synthesis of Nα-Protected Amino and Peptide Acid Aryl Amides via Iodine-Mediated Oxidative Acylation of Nα-Protected Amino and Peptide Thioacids
![Catalytic Behavior of Mono‐N‐Protected Amino‐Acid Ligands in Ligand‐Accelerated C−H Activation by Palladium(II) - Salazar - 2020 - Angewandte Chemie International Edition - Wiley Online Library Catalytic Behavior of Mono‐N‐Protected Amino‐Acid Ligands in Ligand‐Accelerated C−H Activation by Palladium(II) - Salazar - 2020 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/edcd1832-0891-4477-993f-c0f13a67c6aa/anie202002484-toc-0001-m.png)
Catalytic Behavior of Mono‐N‐Protected Amino‐Acid Ligands in Ligand‐Accelerated C−H Activation by Palladium(II) - Salazar - 2020 - Angewandte Chemie International Edition - Wiley Online Library
Mono-N-protected amino acid ligands stabilize dimeric palladium(ii) complexes of importance to C–H functionalization - Chemical Science (RSC Publishing)
![Molecules | Free Full-Text | One-Pot and Catalyst-Free Transformation of N- Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids Molecules | Free Full-Text | One-Pot and Catalyst-Free Transformation of N- Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids](https://pub.mdpi-res.com/molecules/molecules-27-03571/article_deploy/html/images/molecules-27-03571-ag.png?1654853032)
Molecules | Free Full-Text | One-Pot and Catalyst-Free Transformation of N- Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids
![Direct amidations between N-Boc protected β-amino acid and C-protected... | Download Scientific Diagram Direct amidations between N-Boc protected β-amino acid and C-protected... | Download Scientific Diagram](https://www.researchgate.net/publication/277785364/figure/fig5/AS:668867529555970@1536481854427/Direct-amidations-between-N-Boc-protected-b-amino-acid-and-C-protected-b-amino-acid-as.png)
Direct amidations between N-Boc protected β-amino acid and C-protected... | Download Scientific Diagram
![Protecting‐Group‐Free Amidation of Amino Acids using Lewis Acid Catalysts - Sabatini - 2018 - Chemistry – A European Journal - Wiley Online Library Protecting‐Group‐Free Amidation of Amino Acids using Lewis Acid Catalysts - Sabatini - 2018 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0cd142a4-ff3c-43b7-a419-682c0d4aedeb/chem201800372-fig-5004-m.jpg)