Directed Ortho Borylation of Functionalized Arenes Catalyzed by a Silica-Supported Compact Phosphine−Iridium System
An immobilized monophosphine−Ir system, which was prepared in situ from [Ir(OMe)(cod)]2 and a silica-supported, compact phosphine, showed high activities and selectivities for the borylation of aromatic C−H bonds with bis(pinacolato)diboron. This system was effective not only for the borylation of b...
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Published in: | Journal of the American Chemical Society Vol. 131; no. 14; pp. 5058 - 5059 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
American Chemical Society
15-04-2009
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Online Access: | Get full text |
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Summary: | An immobilized monophosphine−Ir system, which was prepared in situ from [Ir(OMe)(cod)]2 and a silica-supported, compact phosphine, showed high activities and selectivities for the borylation of aromatic C−H bonds with bis(pinacolato)diboron. This system was effective not only for the borylation of benzene but also for the ortho borylation of arenes with directing groups, such as ester, amide, sulfonate, acetal, alkoxymethyl, and chloro groups, under mild reaction conditions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja9008419 |