Literature DB >> 21182315

N-aminoazetidinecarboxylic acid: direct access to a small-ring hydrazino acid.

Valérie Declerck1, David J Aitken.   

Abstract

A short and efficient synthesis of the previously unknown N-aminoazetidinecarboxylic acid has been established using a photochemical [2 + 2] cycloaddition strategy starting from 6-azauracil. Chiral derivatization with a nonracemic oxazolidinone provided access to both enantiomers of the title product.

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Year:  2010        PMID: 21182315     DOI: 10.1021/jo102108t

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Synthesis of azetidines via visible-light-mediated intermolecular [2+2] photocycloadditions.

Authors:  Marc R Becker; Emily R Wearing; Corinna S Schindler
Journal:  Nat Chem       Date:  2020-09-23       Impact factor: 24.427

Review 2.  Synthesis of azetidines by aza Paternò-Büchi reactions.

Authors:  Alistair D Richardson; Marc R Becker; Corinna S Schindler
Journal:  Chem Sci       Date:  2020-06-12       Impact factor: 9.825

3.  Novel Aza-Paternò-Büchi Reaction Allows Pinpointing Carbon-Carbon Double Bonds in Unsaturated Lipids by Higher Collisional Dissociation.

Authors:  Andrea Cerrato; Anna Laura Capriotti; Chiara Cavaliere; Carmela Maria Montone; Susy Piovesana; Aldo Laganà
Journal:  Anal Chem       Date:  2022-09-19       Impact factor: 8.008

  3 in total

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