Immonium ion based synthetic methodology: a novel method for the N-methylation of dipeptides and amino acid derivatives via retro aza Diels-Alder reactions

Paul A. Grieco, Ali Bahsas

J. Org. Chem., 1987, 52 (26), pp 5746–5749

DOI: 10.1021/jo00235a021

Publication Date: December 1987

Note: In lieu of an abstract, this is the article's first page.

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Article

Immonium ion based synthetic methodology: a novel method for the N-methylation of dipeptides and amino acid derivatives via retro aza Diels-Alder reactions

Structure–Reactivity Relationships of Zwitterionic 1,3-Diaza-Claisen Rearrangements

Total Synthesis of Cyclosporine: Access to N-Methylated Peptides via Isonitrile Coupling Reactions

Structural and Initial Biological Analysis of Synthetic Arylomycin A₂

Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update

Convenient Synthesis of N-Methylamino Acids Compatible with Fmoc Solid-Phase Peptide Synthesis

Synthetic Preparation of N-Methyl-α-amino Acids

A 1,3-Diaza-Claisen Rearrangement that Affords Guanidines

An Efficient and Practical N-Methylation of Amino Acid Derivatives

Rare-Earth Metal Triflates in Organic Synthesis

Phoriospongin A and B: Two New Nematocidal Depsipeptides from the Australian Marine Sponges Phoriospongia sp. and Callyspongia bilamellata

Direct Mono-N-methylation of Solid-Supported Amino Acids: A Useful Application of the Matteson Rearrangement of α-Aminoalkylboronic Esters

Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease: Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P₁ Glutamine Isosteric Replacements

Preparation, Characterization, and Synthetic Uses of Lanthanide(III) Catalysts Supported on Ion Exchange Resins

Synthesis of Azasugars via Lanthanide-Promoted Aza Diels−Alder Reactions in Aqueous Solution

Enantiospecific Synthesis of Heterocycles from α-Amino Acids

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Immonium ion based synthetic methodology: a novel method for the N-methylation of dipeptides and amino acid derivatives via retro aza Diels-Alder reactions

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