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Synthesis of five-ring-fused azepinone derivatives from bis-isatins via sequential 6π-electrocyclic ring closure, ring expansion, and dehydrogenation process
Bulletin of the Korean Chemical Society ( IF 2.3 ) Pub Date : 2023-01-08 , DOI: 10.1002/bkcs.12672 Sangku Lee 1 , Junseong Lee 2 , Jae Nyoung Kim 2
Bulletin of the Korean Chemical Society ( IF 2.3 ) Pub Date : 2023-01-08 , DOI: 10.1002/bkcs.12672 Sangku Lee 1 , Junseong Lee 2 , Jae Nyoung Kim 2
Affiliation
Five-ring-fused azepinone derivatives were synthesized serendipitously from bis-isatins via sequential 6π-electrocyclic ring closure, ring expansion, and dehydrogenation process in moderate yields (34%–47%). The reaction was carried out in diphenyl ether at 230 °C for 4–12 h under O2 balloon atmosphere.
中文翻译:
通过顺序 6π-电环闭环、扩环和脱氢过程从双靛红合成五环稠合氮杂庚酮衍生物
通过顺序 6π-电环闭环、扩环和脱氢过程,以中等产率 (34%–47%) 从双靛红偶然合成了五环稠合氮杂庚酮衍生物。反应在二苯醚中于 230 °C 在 O 2气球气氛下进行 4-12 小时。
更新日期:2023-01-08
中文翻译:
通过顺序 6π-电环闭环、扩环和脱氢过程从双靛红合成五环稠合氮杂庚酮衍生物
通过顺序 6π-电环闭环、扩环和脱氢过程,以中等产率 (34%–47%) 从双靛红偶然合成了五环稠合氮杂庚酮衍生物。反应在二苯醚中于 230 °C 在 O 2气球气氛下进行 4-12 小时。