2012
DOI: 10.1016/j.tetlet.2012.07.089
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Immobilization of ethylene bis-indenyl ligands on functionalized silica gel

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Cited by 3 publications
(1 citation statement)
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“…In 2002, Nifant’ev et al reported a facile Pd-catalyzed direct arylation of indene with aryl iodides to afford a mixture of 2- and 3-arylindenes in a 4/1 ratio (Scheme a) . The conventional method for the preparation of 3-substituted indenes involves first formation of indenyl lithium, generated in situ by deprotonation of indene with n -butyl lithium and subsequently reaction with electrophiles (Scheme b–d) . This method suffers from several drawbacks, such as the use of very low temperatures, long reaction time, and unsatisfactory regioselectivity.…”
Section: Introductionmentioning
confidence: 99%
“…In 2002, Nifant’ev et al reported a facile Pd-catalyzed direct arylation of indene with aryl iodides to afford a mixture of 2- and 3-arylindenes in a 4/1 ratio (Scheme a) . The conventional method for the preparation of 3-substituted indenes involves first formation of indenyl lithium, generated in situ by deprotonation of indene with n -butyl lithium and subsequently reaction with electrophiles (Scheme b–d) . This method suffers from several drawbacks, such as the use of very low temperatures, long reaction time, and unsatisfactory regioselectivity.…”
Section: Introductionmentioning
confidence: 99%