Chiral Lewis Base Catalyzed Enantioselective Selenocyclization of 1,1-Disubstituted Alkenes: Asymmetric Synthesis of Selenium-Containing 4 H -3,1-Benzoxazines

An enantioselective selenocyclization of 1,1-disubstituted alkenes was achieved for the first time, which is enabled by a novel combination of a chiral BINAM-derived sulfide and an achiral Lewis acid. Various selenium-containing 4 -3,1-benzoxazines, which are widely present in a range of medicinally...

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Veröffentlicht in:Organic letters 2022-06, Vol.24 (22), p.4093-4098
Hauptverfasser: Cao, Ren-Fei, Yu, Lu, Huo, Yu-Xuan, Li, Yao, Xue, Xiao-Song, Chen, Zhi-Min
Format: Artikel
Sprache:eng
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Zusammenfassung:An enantioselective selenocyclization of 1,1-disubstituted alkenes was achieved for the first time, which is enabled by a novel combination of a chiral BINAM-derived sulfide and an achiral Lewis acid. Various selenium-containing 4 -3,1-benzoxazines, which are widely present in a range of medicinally relevant molecules, were readily obtained in moderate to good yields and good to excellent enantioselectivities. A series of tetrasubstituted carbon stereocenters were facilely constructed.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c01731