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An Efficient Synthesis of Nα-Protected Amino and Peptide Acid Aryl Amides via Iodine-Mediated Oxidative Acylation of Nα-Protected Amino and Peptide Thioacids
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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
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Solventless Synthesis of N-Protected Amino Acids in a Ball Mill | ACS Sustainable Chemistry & Engineering
Fmoc-L-Cysteine-(Acetamidomethyl), 5 g, CAS No. 86060-81-3 | Fluorenylmethylene / Fmoc | Amino acids, protected | Amino Acid Derivatives | Amino Acids and Amino Acid Derivatives | Organic & Bioorganic Chemicals | Chemicals | Carl Roth - International
![Scheme 1. The stereoselective transformation of N-protected α-amino... | Download Scientific Diagram Scheme 1. The stereoselective transformation of N-protected α-amino... | Download Scientific Diagram](https://www.researchgate.net/publication/338728650/figure/fig1/AS:849962711674884@1579658310680/Scheme-1-The-stereoselective-transformation-of-N-protected-a-amino-acids-and-their.png)
Scheme 1. The stereoselective transformation of N-protected α-amino... | Download Scientific Diagram
A rapid and efficient one-pot method for the reduction of N-protected α-amino acids to chiral α-amino aldehydes using CDI/DIBAL-H - Organic & Biomolecular Chemistry (RSC Publishing)
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Tertiary-butoxycarbonyl (Boc) – A strategic group for N-protection/deprotection in the synthesis of various natural/unnatural N-unprotected aminoacid cyanomethyl esters - ScienceDirect
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Molecules | Free Full-Text | Synthesis of Chiral TFA-Protected α-Amino Aryl-Ketone Derivatives with Friedel–Crafts Acylation of α-Amino Acid N-Hydroxysuccinimide Ester
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