首页> 外文期刊>Phosphorus, Sulfur, and Silicon and the Related Elements >AgBF4 catalyzed regio- and stereoselective synthesis of trans alpha-vinyl-beta-amino esters via asymmetric addition of siyl dienolate to sulfinylimines
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AgBF4 catalyzed regio- and stereoselective synthesis of trans alpha-vinyl-beta-amino esters via asymmetric addition of siyl dienolate to sulfinylimines

机译:AgBF4通过非对称加入Siemmetric添加到亚磺基胺的不对称和立体选择合成反式α-乙烯基-β-氨基酯

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摘要

AgBF4 catalyzed Mannich-type reactions of siyl dienolate with chiral aryl-substituted (S)-N-tert-butanesulfinylimines has been developed. A class of chiral trans -vinyl--amino esters was obtained in moderate to excellent yields (up to 93%), good diastereoselectiveties (up to 92:8 dr), and complete -site regioselectivity.
机译:已经开发了AgBF4催化SieL芳基取代(S)-N-叔丁沙磺基氨基的SieL dienolate的曼尼希型反应。 在中等至优异的产率(高达93%),良好的非对映异度(高达92:8)和完全的区域选择性中,获得一类手性反式戊基 - 氨基酯。

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