Literature DB >> 25790035

Metal-free nitro-carbocyclization of 1,6-enynes with (t)BuONO and TEMPO.

Xin-Hua Hao1, Pin Gao, Xian-Rong Song, Yi-Feng Qiu, Dong-Po Jin, Xue-Yuan Liu, Yong-Min Liang.   

Abstract

A novel and convenient metal-free nitration and cyclization of 1,6-enynes has been developed. Two C-C bonds and one C-N bond were constructed in one process in this reaction. This transformation is proven to have relatively good functional-group applicability and can be scaled up to gram quantities in satisfactory yields. According to the following experimental facts and related literature reports, a radical pathway was involved in this transformation.

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Year:  2015        PMID: 25790035     DOI: 10.1039/c5cc00872g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  K2S2O8-mediated radical cyclisation of 2-alkynylthioanisoles or -selenoanisoles: a green and regioselective route to 3-nitrobenzothiophenes and benzoselenophenes.

Authors:  Shi-Chao Lu; Botao Wu; Shi-Peng Zhang; Ya-Ling Gong; Shu Xu
Journal:  RSC Adv       Date:  2020-05-19       Impact factor: 3.361

  1 in total

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