Literature DB >> 35900638

New oxacycles on the block: benzodioxepinones via a Passerini reaction.

Michael Fragkiadakis1, Marios Zingiridis1, Edward Loukopoulos1, Constantinos G Neochoritis2.   

Abstract

Oxacycles and benzoxepanes are privileged motifs present in a variety of natural products and functional molecules. However, their synthetic access is limited. Here, we demonstrate a rapid synthesis of unprecedented benzoxepanes from readily available starting materials in one step via a Passerini multicomponent reaction. The reaction proceeds smoothly under mild reaction conditions. We have obtained a single-crystal X-ray structure, revealing a butterfly conformation, combined with useful structural features. In addition, we have performed both a full interaction map on the X-ray structure and a profile analysis of a virtual library based on the proposed scaffold with a special focus on certain physicochemical parameters to demonstrate their potential usage in drug discovery.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Entities:  

Keywords:  Dioxepinones; Multicomponent reactions (MCRs); Oxacycles; Passerini reaction; Rule of five (Ro5)

Year:  2022        PMID: 35900638     DOI: 10.1007/s11030-022-10502-9

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   3.364


  17 in total

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