期刊文献+

Studies on Diastereoselective Intramolecular meta-Cycloaddition of Arene to Olefin (Part Ⅱ)

Studies on Diastereoselective Intramolecular meta-Cycloaddition of Arene to Olefin (Part Ⅱ)
下载PDF
导出
摘要 The photoinduced intramolecular meta-cycloaddition of bichromophores 1a-1d gave diastereoselectively two types of adducts 2a-2d and 3a-3d respectively. The observed stereochemistry of cycloaddition is rationalized in terms of hydrogen bond effect induced by the 4hydroxy group in the 5-phenylpent-1-ene skeleton. The photoinduced intramolecular meta-cycloaddition of bichromophores 1a-1d gave diastereoselectively two types of adducts 2a-2d and 3a-3d respectively. The observed stereochemistry of cycloaddition is rationalized in terms of hydrogen bond effect induced by the 4hydroxy group in the 5-phenylpent-1-ene skeleton.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第4期321-323,共3页 中国化学快报(英文版)
关键词 Arene Olefin meta-Cycloaddition DIASTEREOSELECTIVITY Arene, Olefin meta-Cycloaddition Diastereoselectivity
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部