Publication
Title
Synthesis of (hetero)arylated pyridazin-3(2H)-ones via Negishi reaction involving zincated pyridazin-3(2H)-ones
Author
Abstract
Zincated pyridazin-3(2H)-ones generated via brominemagnesium exchange followed by transmetalation using ZnCl2 or via lactam-directed ortho C4-H zincation with TMPZnCl·LiCl have been synthesized. These in situ created organometallics can be used in Negishi reactions with iodo(hetero)arenes delivering a new approach toward (hetero)arylpyridazin-3(2H)-ones.
Language
English
Source (journal)
The journal of organic chemistry. - Washington, D.C., 1936, currens
Publication
Washington, D.C. : 2011
ISSN
0022-3263 [print]
1520-6904 [online]
DOI
10.1021/JO201587J
Volume/pages
76 :23 (2011) , p. 9648-9659
ISI
000297274800012
Full text (Publisher's DOI)
Full text (publisher's version - intranet only)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identifier
Creation 19.12.2011
Last edited 15.11.2022
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