Broad-spectrum radical cyclizations boosted by polarity matching.: Carbonylative access to α-stannylmethylene lactams from azaenynes and CO
Broad-spectrum radical cyclizations boosted by polarity matching.: Carbonylative access to α-stannylmethylene lactams from azaenynes and CO
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DOI:
10.1021/ja034896u
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发表时间:
2003-05-14
影响因子:
15
通讯作者:
Komatsu, M
中科院分区:
文献类型:
--
作者:
Ryu, I;Miyazato, H;Komatsu, M
Free-radical mediated stannylcarbonylation of azaenynes provides a general [n+ 1]-type annulation approach leading to α-stannylmethylene lactams. The cyclization is unusual in its breadth, covering 4-exo, 5-exo, 6-exo, 7-exo, and 8-exo modes.