Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans.

Aziridines formed upon treatment of allylic carbamates and homoallylic sulfamates with Rh(II) carboxylate catalysts under oxidative conditions are trapped by suitably-disposed hydroxyl groups to give functionalised tetrahydrofurans.

書誌詳細
主要な著者: Unsworth, W, Clark, N, Ronson, T, Stevens, K, Thompson, A, Lamont, S, Robertson, J
フォーマット: Journal article
言語:English
出版事項: 2014