首页> 外文期刊>Organic letters >Catalytic enantioselective intermolecular cycloaddition of 2-diazo-3,6-diketoester-derived carbonyl ylides with alkynes and styrenes using chiral dirhodium(II) carboxylates
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Catalytic enantioselective intermolecular cycloaddition of 2-diazo-3,6-diketoester-derived carbonyl ylides with alkynes and styrenes using chiral dirhodium(II) carboxylates

机译:手性二羧酸(II)羧酸酯与2-炔基和苯乙烯的2-重氮-3,6-二酮酸酯衍生的羰基烷基化物的对映选择性分子间环加成反应

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摘要

Dirhodium(II) tetrakis[N-tetrachlorophthaloyl-(S)-tert-leucinate], Rh-2(S-TCPTTL)(4), is an exceptionally effective catalyst for enantioselective tandem carbonyl ylide formation-cycloaddition reactions of 2-diazo-3,6-diketoesters with arylacetylene, alkoxyacetylene, and styrene dipolarophiles, providing cycloadducts in good to high yields and with enantioselectivities of up to 99% ee as well as with perfect exo diastereoselectivity for styrenes.
机译:四(N-四氯邻苯二甲酰-(S)-叔亮氨酸酯)铑(II)Rh-2(S-TCPTTL)(4)是对2-重氮基-对映选择性串联羰基内酯形成-环加成反应非常有效的催化剂具有芳基乙炔,烷氧基乙炔和苯乙烯双极性亲和剂的3,6-二酮酸酯,提供高至高收率的对映体加​​成物,对映选择性高达99%ee,并且对苯乙烯具有完美的对映非对映选择性。

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