期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 88, 期 11, 页码 6750-6764出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.3c00035
关键词
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A Pd-catalyzed cascade annulation process involving C-C bond formation and 1,6-conjugate addition for pi-extended benzofulvenes is described. The process is compatible with various functionalities of p-quinone methides and internal alkynes, resulting in diverse pi-extended benzofulvenes. Furthermore, this strategy can also be applied to aryne annulation with p-quinone methides.
A Pd-catalyzed cascade annulation process comprising C-C bond formation followed by 1,6-conjugate addition for pi extended benzofulvenes is reported. This process is compatible with a wide range of functionalities for both the p-quinone methides and internal alkynes, leading to diverse pi-extended benzofulvenes. Additionally, this strategy is also applicable for aryne annulation with p-quinone methides.
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