In:
Advanced Synthesis & Catalysis, Wiley, Vol. 363, No. 8 ( 2021-04-13), p. 2148-2156
Abstract:
Herein, we report the [Bis(trifluoroacetoxy)iodo]benzene mediated C−H bond arylselenylation of 4 H ‐Pyrido‐[1,2‐ a ]‐Pyrimidin‐4‐ones using readily available organodiselenides. This methodology is scalable and permits for the generation of a broad spectrum of functionally and structurally diverse selenoether derivatives in very promising yields (up to 98%). Notably, this protocol proceeds at ambient conditions and in the absence of a metal. The application of this methodology for the facile synthesis of ArSe substituted 5 H ‐thiazolo‐pyrido[3,2‐ a ]pyrimidin‐4‐ones is also demonstrated. magnified image
Type of Medium:
Online Resource
ISSN:
1615-4150
,
1615-4169
DOI:
10.1002/adsc.202001426
Language:
English
Publisher:
Wiley
Publication Date:
2021
detail.hit.zdb_id:
2041384-1
detail.hit.zdb_id:
2033084-4
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