Literature DB >> 25553911

Expedient access to α,β-difunctionalized azepenes using α-halo eneformamides: application to the one-pot synthesis of 2-benzazepanes.

Daniel P Bassler1, Laura Spence, Amir Alwali, Oliver Beale, Timothy K Beng.   

Abstract

The regioselective synthesis of α,β-difunctionalized (alkenyl, aryl, sulfonyl, allyl, or alkynyl) azepenes has been accomplished through α-halo eneformamides. A successful implementation of the vicinal functionalization strategy has led to a one-pot synthesis of 2-benzazepanes whose benzenoid portion is highly functionalized.

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Year:  2015        PMID: 25553911     DOI: 10.1039/c4ob02183e

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


  2 in total

1.  Leveraging the 1,3-azadiene-anhydride reaction for the synthesis of functionalized piperidines bearing up to five contiguous stereocenters.

Authors:  Jorge Garcia; Jane Eichwald; Jayme Zesiger; Timothy K Beng
Journal:  RSC Adv       Date:  2021-12-20       Impact factor: 3.361

2.  Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli-Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides.

Authors:  Timothy K Beng; Abdikani Omar Farah; Victoria Shearer
Journal:  RSC Adv       Date:  2020-10-07       Impact factor: 4.036

  2 in total

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