A chiral aldehyde-induced tandem conjugated addition–lactamization reaction for constructing fully substituted pyroglutamic acids

A catalytic asymmetric tandem reaction including a chiral aldehyde catalyzed conjugated addition and an intramolecular lactamization is reported in this work. Under the optimal reaction conditions, various fully substituted pyroglutamic acids bearing three vicinal chiral centers were generated in go...

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Veröffentlicht in:Organic Chemistry Frontiers 2022-03, Vol.9 (5), p.1422-1426
Hauptverfasser: Wang, Wen-Zhe, Shen, Hao-Ran, Liao, Jian, Wen, Wei, Guo, Qi-Xiang
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Sprache:eng
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Zusammenfassung:A catalytic asymmetric tandem reaction including a chiral aldehyde catalyzed conjugated addition and an intramolecular lactamization is reported in this work. Under the optimal reaction conditions, various fully substituted pyroglutamic acids bearing three vicinal chiral centers were generated in good-to-excellent yields and stereoselectivities. A reasonable reaction mechanism is proposed to illustrate the observed stereoselective control results.
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/D1QO01923F