Literature DB >> 30452059

Intermolecular alkene difunctionalizations for the synthesis of saturated heterocycles.

Navdeep Kaur1, Fan Wu, Nur-E Alom, Jeewani P Ariyarathna, Shannon J Saluga, Wei Li.   

Abstract

Saturated heterocycles are important structural motifs in a range of pharmaceuticals and agrochemicals. As a result of their importance, syntheses of these molecules have been extensively investigated. Despite the progress in this area, the most adopted strategies are still often characterized with inefficiency or relying on functionalizations with specialized precursors and pre-existing cores. This review highlights a dynamic synthetic strategy for the direct synthesis of saturated heterocycles from intermolecular alkene difunctionalizations. These coupling processes are highly modular, and therefore, offer perhaps the most convenient means to prepare diverse heterocyclic structures in compound libraries for bioactivity evoluations.

Entities:  

Year:  2019        PMID: 30452059     DOI: 10.1039/c8ob02443j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  Lewis Acid-Catalyzed Halonium Generation for Morpholine Synthesis and Claisen Rearrangement.

Authors:  Jeewani P Ariyarathna; Nur-E Alom; Leo P Roberts; Navdeep Kaur; Fan Wu; Wei Li
Journal:  J Org Chem       Date:  2022-02-10       Impact factor: 4.198

Review 2.  Recent Advances in 1,2-Amino(hetero)arylation of Alkenes.

Authors:  Yungeun Kwon; Qiu Wang
Journal:  Chem Asian J       Date:  2022-05-03

3.  General Pyrrolidine Synthesis via Iridium-Catalyzed Reductive Azomethine Ylide Generation from Tertiary Amides and Lactams.

Authors:  Ken Yamazaki; Pablo Gabriel; Graziano Di Carmine; Julia Pedroni; Mirxan Farizyan; Trevor A Hamlin; Darren J Dixon
Journal:  ACS Catal       Date:  2021-06-09       Impact factor: 13.084

4.  Bifunctional sulfilimines enable synthesis of multiple N-heterocycles from alkenes.

Authors:  Qiang Cheng; Zibo Bai; Srija Tewari; Tobias Ritter
Journal:  Nat Chem       Date:  2022-07-25       Impact factor: 24.274

  4 in total

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