
Tetrahedron Letters p. 1773 - 1776 (1997)
Update date:2022-08-03
Topics:
Nguyen, Van-Ha
Nishino, Hiroshi
Kurosawa, Kazu
Molecular oxygen trapping reaction of alkenes with 2,3-pyrrolidinedione derivatives was developed using a Mn(III)-induced oxidation system. Alkenes and 2,3-pyrrolidinediones were treated with manganese(III) acetate in acetic acid under a stream of dry air, giving 1-hydroxy-8-aza-2,3-dioxabicyclo[4.3.0]nonan-9-ones in good yields, The reaction involved molecular oxygen trapping of radicals which were formed by the addition of pyrrolidinedione radicals induced by Mn(III) to alkenes.
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Doi:10.1021/ja970285o
(1997)Doi:10.1039/b603015g
(2006)Doi:10.1080/00304949709355199
(1997)Doi:10.3987/COM-96-7700
(1997)Doi:10.1016/S0008-6215(97)00341-8
(1997)Doi:10.1016/S0957-4166(97)00064-5
(1997)