Expansion of annulation of allenoates with trifluoroketones : Synthesis of trifluoromethylated dihydropyrans

Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review

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Detail(s)

Original languageEnglish
Pages (from-to)315-321
Journal / PublicationSynthetic Communications
Volume50
Issue number3
Online published14 Jan 2020
Publication statusPublished - 2020

Link(s)

DOI

DOI
Check@CityULib
Link to Scopus https://www.scopus.com/record/display.uri?eid=2-s2.0-85077987616&origin=recordpage
Permanent Link https://scholars.cityu.edu.hk/en/publications/publication(325e45d4-7508-443d-83c1-67384a483dfb).html

Abstract

The DABCO-catalyzed [2 + 2] annulation of allenoates with trifluoroketones could be expanded to [4 + 2] annulation to synthesize trifluoromethylated dihydropyrans with trifluoromethyl oxadienes as the electrophilic annulation partners.

Research Area(s)

  • Allenoates, dihydropyrans, trifluoromethyl oxadienes, [4 + 2] annulation

Citation Format(s)

[ RIS ] [ BibTeX ]

Expansion of annulation of allenoates with trifluoroketones : Synthesis of trifluoromethylated dihydropyrans. / Wang, Tong; Liu, Yanpeng; Xu, Jinyi.

In: Synthetic Communications, Vol. 50, No. 3, 2020, p. 315-321.

Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review