Literature DB >> 31840516

Catalytic Enantioselective Synthesis of 1,4-Benzodioxepines.

Xi Zou1, Guangwu Sun1, Hai Huang2, Jinping Wang1, Wen Yang1, Jianwei Sun3.   

Abstract

An efficient organocatalytic enantioselective synthesis of chiral 1,4-benzodioxepines is described. By proper incorporation of an intramolecular oxetane desymmetrization process, a range of benzylic alcohols bearing an internal oxetane reacted in the presence of a suitable chiral phosphoric acid catalyst to form chiral 1,4-benzodioxepines with high enantioselectivity. This process provides a new catalytic asymmetric example of direct synthesis of seven-membered heterocycles with good stereocontrol.

Entities:  

Year:  2019        PMID: 31840516     DOI: 10.1021/acs.orglett.9b04244

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

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

Authors:  Michael Fragkiadakis; Marios Zingiridis; Edward Loukopoulos; Constantinos G Neochoritis
Journal:  Mol Divers       Date:  2022-07-28       Impact factor: 3.364

2.  Dynamic kinetic resolution of transient hemiketals: a strategy for the desymmetrisation of prochiral oxetanols.

Authors:  Alexander Sandvoß; Henning Maag; Constantin G Daniliuc; Dieter Schollmeyer; Johannes M Wahl
Journal:  Chem Sci       Date:  2022-05-04       Impact factor: 9.969

3.  Identifying the true origins of selectivity in chiral phosphoric acid catalyzed N-acyl-azetidine desymmetrizations.

Authors:  Pier Alexandre Champagne
Journal:  Chem Sci       Date:  2021-11-23       Impact factor: 9.825

4.  Unexpected Isomerization of Oxetane-Carboxylic Acids.

Authors:  Bohdan Chalyk; Anastasiia Grynyova; Kateryna Filimonova; Tymofii V Rudenko; Dmitry Dibchak; Pavel K Mykhailiuk
Journal:  Org Lett       Date:  2022-06-29       Impact factor: 6.072

  4 in total

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