Literature DB >> 30265556

N-Arylation of DABCO with Diaryliodonium Salts: General Synthesis of N-Aryl-DABCO Salts as Precursors for 1,4-Disubstituted Piperazines.

Dmitry I Bugaenko1, Marina A Yurovskaya1, Alexander V Karchava1.   

Abstract

Employing DABCO as a substrate, aryl(mesityl)iodonium triflates are introduced as arylating agents for a tertiary sp3-nitrogen. Mild conditions and exceptional selectivity of the aryl group transfer allow unprecedented N-aryl-DABCO salts to be obtained, bearing substituents of different electronic natures. This metal-free methodology has no analogy among known transition-metal-based reactions. The utility of isolated N-aryl-DABCO salts is demonstrated for the preparation of flibanserin.

Entities:  

Year:  2018        PMID: 30265556     DOI: 10.1021/acs.orglett.8b02676

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


  2 in total

Review 1.  DABCO bond cleavage for the synthesis of piperazine derivatives.

Authors:  Azim Ziyaei Halimehjani; Elham Badali
Journal:  RSC Adv       Date:  2019-11-08       Impact factor: 4.036

2.  Sulfonylation of 1,4-Diazabicyclo[2.2.2]octane: Charge-Transfer Complex Triggered C-N Bond Cleavage.

Authors:  Ying Fu; Qin-Shan Xu; Quan-Zhou Li; Ming-Peng Li; Chun-Zhao Shi; Zhengyin Du
Journal:  ChemistryOpen       Date:  2019-01-28       Impact factor: 2.911

  2 in total

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