A Short and Efficient Synthesis of (R)‐(‐)‐Sporochnol A (I).

Abstract

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Chemo, stereo, and regioselective addition of α‐(2‐methoxyaryl)‐N‐aryl nitrones to diarylidineacetone: Synthesis of novel isoxazolidines

“…Among all five membered heterocyclic systems, isoxazolidines attracted considerable attention of organic chemists and biochemists due to their potential biological activities [2][3][4][5]. In recent years, an enormous number of articles have been published highlighting the synthesis of isoxazolidines via 1,3-dipolar cycloaddition reactions [6][7][8][9][10]. These cycloadducts, isoxazolidines have been used as templates to generate -amino alcohols through reductive cleavage of the N-O bond, which are potential precursors for the synthesis of several natural products such as -lactam antibiotics and alkaloids [11].…”