Literature DB >> 23186000

Direct synthesis of substituted naphthalenes from 1,3-dicarbonyl compounds and 1,2-bis(halomethyl)benzenes including a novel rearrangement aromatization of benzo[c]oxepine.

Jun-gang Wang1, Meng Wang, Jia-chen Xiang, Yan-ping Zhu, Wei-jian Xue, An-xin Wu.   

Abstract

An unexpected rearrangement aromatization of benzo[c]oxepine has been revealed to synthesize substituted naphthalenes. This observation was further exploited to develop an efficient approach for the construction of naphthalenes from simple and commercially available 1,3-dicarbonyl compounds and 1,2-bis(halomethyl)benzene compounds via a new domino reaction sequence.

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Year:  2012        PMID: 23186000     DOI: 10.1021/ol302950w

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


  2 in total

1.  Crystal structures of two bis-(iodo-meth-yl)benzene derivatives: similarities and differences in the crystal packing.

Authors:  C John McAdam; Lyall R Hanton; Stephen C Moratti; Jim Simpson
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-11-18

2.  Ethyl 2-(4-methyl-benzo-yl)-2,3-dihydro-1H-indene-2-carboxyl-ate.

Authors:  Jiachen Xiang; Tingting Hu; Jungang Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-03-06
  2 in total

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