ChemInform Abstract: Construction of Oxadiazepines via Lewis Acid‐Catalyzed Tandem 1,5‐Hydride Shift/Cyclization
Lewis acid‐promoted reactions of pyrrolidine‐ or tetrahydroisoquinoline‐containing nitrones afford oxadiazepines in good yields.
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| Veröffentlicht in: | ChemInform 2016-02, Vol.47 (9), p.no-no |
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| container_issue | 9 |
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| container_title | ChemInform |
| container_volume | 47 |
| creator | Chang, Yong‐Zhi Li, Ming‐Lei Zhao, Wen‐Feng Wen, Xiaoan Sun, Hongbin Xu, Qing‐Long |
| description | Lewis acid‐promoted reactions of pyrrolidine‐ or tetrahydroisoquinoline‐containing nitrones afford oxadiazepines in good yields. |
| doi_str_mv | 10.1002/chin.201609194 |
| format | Article |
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| language | eng |
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| source | Wiley Online Library Journals Frontfile Complete |
| subjects | catalysis, phase‐transfer catalysis multi‐membered O,N,S‐heterocycles (with at least 2 different heteroatoms) ring closure reactions, annulation reactions |
| title | ChemInform Abstract: Construction of Oxadiazepines via Lewis Acid‐Catalyzed Tandem 1,5‐Hydride Shift/Cyclization |
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