Literature DB >> 12919062

Synthesis of tetrasubstituted naphthalenes by palladium-catalyzed reaction of aryl iodides with internal alkynes.

Satoshi Kawasaki1, Tetsuya Satoh, Masahiro Miura, Masakatsu Nomura.   

Abstract

The 1:2 coupling of aryl iodides with acetylenedicarboxylate esters and diphenylacetylene efficiently proceeds in the presence of a palladium catalyst with use of silver carbonate as base to produce the corresponding tetrasubstituted naphthalenes.

Entities:  

Year:  2003        PMID: 12919062     DOI: 10.1021/jo0346656

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Highly efficient route to fused polycyclic aromatics via palladium-catalyzed aryne annulation by aryl halides.

Authors:  Zhijian Liu; Richard C Larock
Journal:  J Org Chem       Date:  2007-01-05       Impact factor: 4.354

2.  Benzene construction via Pd-catalyzed cyclization of 2,7-alkadiynylic carbonates in the presence of alkynes.

Authors:  Yuchen Zhang; Wangteng Wu; Chunling Fu; Xin Huang; Shengming Ma
Journal:  Chem Sci       Date:  2018-12-19       Impact factor: 9.825

  2 in total

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