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Broad-spectrum radical cyclizations boosted by polarity matching. Carbonylative access to alpha-stannylmethylene lactams from azaenynes and CO
Authors:Ryu Ilhyong  Miyazato Hironari  Kuriyama Hiroki  Matsu Kazutoshi  Tojino Mami  Fukuyama Takahide  Minakata Satoshi  Komatsu Mitsuo
Institution:Department of Chemistry, Faculty of Arts and Sciences, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan. ryu@ms.cias.osakafu-u.ac.jp
Abstract:Free-radical mediated stannylcarbonylation of azaenynes provides a general n + 1]-type annulation approach leading to alpha-stannylmethylene lactams. The cyclization is unusual in its breadth, covering 4-exo, 5-exo, 6-exo, 7-exo, and 8-exo modes.
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