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author:

Wu, W. (Wu, W..) [1] | Han, X. (Han, X..) [2] | Weng, Z. (Weng, Z..) [3]

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Abstract:

A new strategy for the construction of pertrifluoromethyl pyridazine derivatives is presented. The tandem reaction starts from the condensation of arenediazonium salts with hexafluoroacetylacetone leading to the formation of pertrifluoromethyl pyridazinols, which readily undergo electrophilic substitution reactions with phenols to afford benzo[5,6]chromeno[3,4-c]pyridazine products in the presence of concd H2SO4. © 2020 the Partner Organisations.

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Community:

  • [ 1 ] [Wu, W.]Key Laboratory of Molecule Synthesis and Function Discovery, Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Han, X.]Testing and Analysis Center, Soochow University, Suzhou, 215123, China
  • [ 3 ] [Weng, Z.]Key Laboratory of Molecule Synthesis and Function Discovery, Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou University, Fuzhou, 350108, China

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Source :

Organic Chemistry Frontiers

ISSN: 2052-4110

Year: 2020

Issue: 21

Volume: 7

Page: 3499-3504

5 . 2 8 1

JCR@2020

4 . 6 0 0

JCR@2023

ESI HC Threshold:160

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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