Lewis acid-catalyzed tandem cyclization of in situ generated o-quinone methides and arylsulfonyl hydrazides for a one-pot entry to 3-sulfonylbenzofurans Article

Meng, Fan-Xiao, Wang, Ruo-Nan, Huang, Hong-Li et al. (2019). Lewis acid-catalyzed tandem cyclization of in situ generated o-quinone methides and arylsulfonyl hydrazides for a one-pot entry to 3-sulfonylbenzofurans . ORGANIC CHEMISTRY FRONTIERS, 6(24), 3929-3933. 10.1039/c9qo01196j

International Collaboration

cited authors

  • Meng, Fan-Xiao; Wang, Ruo-Nan; Huang, Hong-Li; Gong, Shu-Wen; Li, Qian-Li; Zhang, Shao-Liang; Ma, Chun-Lin; Li, Chen-Zhong; Du, Ji-Yuan

sustainable development goals

authors

publication date

  • December 21, 2019

published in

keywords

  • ALCOHOLS
  • ALLENIC ESTERS
  • ANNULATION
  • ASYMMETRIC-SYNTHESIS
  • BETA-DICARBONYLS
  • Chemistry
  • Chemistry, Organic
  • DIELS-ALDER REACTIONS
  • ENANTIOSELECTIVE SYNTHESIS
  • FACILE SYNTHESIS
  • INTRAMOLECULAR 4+2 CYCLOADDITION
  • Physical Sciences
  • SULFONYL
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • ROYAL SOC CHEMISTRY

start page

  • 3929

end page

  • 3933

volume

  • 6

issue

  • 24