Mono-N-protected amino acid ligands stabilize dimeric palladium(ii) complexes of importance to C–H functionalization - Chemical Science (RSC Publishing)
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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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Direct amidations between N-Boc protected β-amino acid and C-protected... | Download Scientific Diagram
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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
![Tertiary-butoxycarbonyl (Boc) – A strategic group for N-protection/deprotection in the synthesis of various natural/unnatural N-unprotected aminoacid cyanomethyl esters - ScienceDirect Tertiary-butoxycarbonyl (Boc) – A strategic group for N-protection/deprotection in the synthesis of various natural/unnatural N-unprotected aminoacid cyanomethyl esters - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403918312590-ga1.jpg)
Tertiary-butoxycarbonyl (Boc) – A strategic group for N-protection/deprotection in the synthesis of various natural/unnatural N-unprotected aminoacid cyanomethyl esters - ScienceDirect
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
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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