Catalytic C-H bond addition of pyridines to allenes by a rare-Earth catalyst.
نویسندگان
چکیده
The catalytic C-H addition of pyridines to allenes has been achieved for the first time by using a half-sandwich scandium catalyst, thus constituting a straightforward and atom-economical route for the synthesis of alkenylated pyridine derivatives. The reaction proceeded regio- and stereoselectively, affording a new family of alkenylated pyridine compounds which are otherwise difficult to synthesize. A cationic Sc-η(2) -pyridyl species was isolated and confirmed to be a key catalyst species in this transformation.
منابع مشابه
Scandium-catalysed intermolecular hydroaminoalkylation of olefins with aliphatic tertiary amines† †Electronic supplementary information (ESI) available: Full experimental details for catalytic procedures and characterization data. See DOI: 10.1039/c6sc02129h Click here for additional data file.
A homoleptic scandium trialkyl complex in combination with a borate compound served as an excellent catalyst for the C–H addition of aliphatic tertiary amines to olefins. This highly regiospecific, 100% atom efficient C–H bond alkylation reaction was applicable to a wide variety of tertiary amines and olefins, including functionalised styrenes and unactivated a-olefins. This work represents the...
متن کاملScandium-catalysed intermolecular hydroaminoalkylation of olefins with aliphatic tertiary amines.
A homoleptic scandium trialkyl complex in combination with a borate compound served as an excellent catalyst for the C-H addition of aliphatic tertiary amines to olefins. This highly regiospecific, 100% atom efficient C-H bond alkylation reaction was applicable to a wide variety of tertiary amines and olefins, including functionalised styrenes and unactivated α-olefins. This work represents the...
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ورودعنوان ژورنال:
- Chemistry
دوره 21 23 شماره
صفحات -
تاریخ انتشار 2015