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Preparation and crystal structures of two 3-anthracenyl isoxazolyl Sulfonamides

机译:两种3-蒽基异恶唑基磺酰胺的制备及晶体结构

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摘要

Lateral metalation and oxidation of 3-(9'-anthryl)-isoxazoles (1), using Davis' oxaziridine (6), produced the desired hydroxylation (2), along with sulfonamide adduct (3), and in the case of the use of butyl lithium as base, butyl addition products (4) and (5). Structures of isoxazole sulfonamides (3a) and (5a), were obtained as the SR/RS-diastereomer, however, studies indicate that this is a consequence of the crystallization process. Metalation studies with isoxazole (8) demonstrate that hydroxylation (9), can be carried out cleanly, minimizing formation of (10), using camphorsulfonyloxaziridine (7) as an electrophile.
机译:使用Davis'恶唑烷(6)进行3-(9'-蒽基)-异恶唑(1)的侧向金属化和氧化反应,可产生所需的羟基化反应(2),以及磺酰胺加合物(3),在使用时丁基锂作为碱,丁基加成产物(4)和(5)。获得了异恶唑磺酰胺(3a)和(5a)的结构,作为SR / RS-非对映异构体,但是研究表明,这是结晶过程的结果。使用樟脑磺酰基恶唑烷(7)作为亲电试剂,用异恶唑(8)进行的金属化研究表明,可以干净地进行羟基化(9),最大程度地减少(10)的形成。

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