Literature DB >> 31742420

Mild Intramolecular Ring Opening of Oxetanes.

Lindsey G DeRatt1, Edward C Lawson1, Chao-Yuan Wang1, Scott D Kuduk1.   

Abstract

Oxetanes have been increasingly used as stable motifs in medicinal chemistry as well as versatile synthetic intermediates. Herein, an intramolecular ring opening of oxetane carboxamides with mild nucleophiles, such as nitrogen heterocycles, is presented. The reaction proceeds under metal-free basic conditions which is highly unusual in ring opening reactions of oxetanes. Amide formation and oxetane ring opening/cyclization in a one-pot approach affords high levels of molecular complexity in a single step from simple, readily available substrates.

Entities:  

Year:  2019        PMID: 31742420     DOI: 10.1021/acs.orglett.9b03810

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


  3 in total

1.  Oxetan-3-ols as 1,2-bis-Electrophiles in a Brønsted-Acid-Catalyzed Synthesis of 1,4-Dioxanes.

Authors:  Juan J Rojas; Elena Torrisi; Maryne A J Dubois; Riashat Hossain; Andrew J P White; Giovanni Zappia; James J Mousseau; Chulho Choi; James A Bull
Journal:  Org Lett       Date:  2022-03-21       Impact factor: 6.005

2.  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

3.  3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions.

Authors:  Zengwei Lai; Renwei Zhang; Qiang Feng; Jianwei Sun
Journal:  Chem Sci       Date:  2020-09-08       Impact factor: 9.825

  3 in total

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