Palladium-Catalyzed Ullmann Cross-Coupling of β-Iodoenones and β-Iodoacrylates with o-Halonitroarenes or o-Iodobenzonitriles and Reductive Cyclization of the Resulting Products To Give Diverse Heterocyclic Systems
Author(s) -
Faiyaz Khan,
Michael Dlugosch,
Xin Liu,
Marium Khan,
Martin G. Banwell,
Jas S. Ward,
Paul D. Carr
Publication year - 2018
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.8b01015
Subject(s) - chemistry , palladium , catalysis , reductive elimination , derivative (finance) , coupling (piping) , coupling reaction , ullmann reaction , combinatorial chemistry , medicinal chemistry , stereochemistry , organic chemistry , mechanical engineering , financial economics , engineering , economics
The palladium-catalyzed Ullmann cross-coupling of β-iodoenones and β-iodoacrylates such as 5 (X = I) with o-halonitroarenes and o-iodobenzonitriles including 2 affords products such as compound 7. These can be engaged in a range of reductive cyclization reactions leading to heterocyclic frameworks such as 3,4-benzomorphan derivative 43.
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