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Coupling of alkynols and a phenyl group to a novel η5-dihydronaphthalenide ligand on a ruthenium template
Author(s) -
J. Cubrilo,
Rainer F. Winter,
Dietrich Gudat
Publication year - 2004
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/b412052c
Subject(s) - ruthenium , tetraphenylborate , ligand (biochemistry) , stoichiometry , coupling (piping) , methylene , chemistry , group (periodic table) , combinatorial chemistry , sodium tetraphenylborate , coupling reaction , medicinal chemistry , organic chemistry , materials science , catalysis , ion , biochemistry , receptor , metallurgy
We report the highly selective assembly of unprecedented eta5-1-methylene-1,2-dihydronaphthalenide ligands from the stoichiometric coupling of a phenyl group and two equivalents of disubstituted propargylic alcohols; in this reaction, tetraphenylborate acts as a phenylating agent.

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