Question

帮忙专业化学翻译下：

A divergent synthetic approach to new sultams utilizing intramolecular oxa-Michael and Baylis-Hillman reactions of readily prepared vinyl sulfonamides and suitably protected amino alcohols, is reported. A variety of seven- and eight-membered ring sultam scaffolds were synthesized using oxa-Michael pathways, whereas both five- and six-membered rings were synthesized using Baylis-Hillman methods. Baylis-Hillman reactions proceed with good to excellent levels of diastereoselectivity, and oxa-Michael reactions leading to eight-membered ring sultams provide empirical evidence validating 8-endo-trig cyclization pathways.
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Answer 1

A divergent synthetic approach to new sultams utilizing intramolecular oxa-Michael and Baylis-Hillman reactions of readily prepared vinyl sulfonamides and suitably protected amino alcohols, is reported.据报道现已经发明了一种新磺内酰胺的扩散合成方法，这种方法是利用预制备的乙烯基磺胺以及，经适当保护的氨基乙醇之间的oxa-Michael分子内加成反应和贝里斯-希尔曼反应。

A variety of seven- and eight-membered ring sultam scaffolds were synthesized using oxa-Michael pathways, whereas both five- and six-membered rings were synthesized using Baylis-Hillman methods.
通过oxa-Michael反应，可以合成各种七元环和八元环的磺内酰胺支架，然而五元环和六元环的磺内酰胺是通过贝里斯-希尔曼反应的方法来合成的。

Baylis-Hillman reactions proceed with good to excellent levels of diastereoselectivity, and oxa-Michael reactions leading to eight-membered ring sultams provide empirical evidence validating 8-endo-trig cyclization pathways.
随着非对应立体选择性由优良级别向优秀级别的转变，贝里斯-希尔曼反应继续进行着；生成八元环磺内酰胺的oxa-Michael反应提供了可以证实8-琼脂-3-环环化的实验证据

Answer 2

使翻译的软件翻译一下

Answer 3

一个不同的合成方法，利用新sultams分子氧杂迈克和磺胺类药物和乙烯随时准备适当的保护氨基醇的Baylis - Hillman反应，报道。阿七和八元环sultam支架，而使用了各种合成同时五和六元环氧杂迈克尔途径，用合成的Baylis - Hillman方法。的Baylis - Hillman反应进行良好的非对映选择性优良水平，氧杂Michael反应，导致八元环sultams提供实验证据证实8远藤- trig的环化途径。