化学
区域选择性
核磁共振波谱
环加成
晶体结构
碳-13核磁共振
立体化学
计算化学
有机化学
催化作用
作者
Josef Breu,Peter Höcht,Uwe Rohr,J. Schatz,Jürgen Sauer
标识
DOI:10.1002/(sici)1099-0690(199812)1998:12<2861::aid-ejoc2861>3.0.co;2-c
摘要
[4+2] Cycloadditions of thiobenzophenones 1a and thiofluorenones 2 with cyclic and open-chain dienes gave cycloadducts in high yields. Assignment of the product structure especially the regiochemistry of the cycloadditions involved 1H- and 13C-NMR spectroscopy, and single-crystal structure determination.
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