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Organocatalyzed Enantioselective Direct Mannich Reaction of α‑Styrylacetates

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Organocatalyzed_Enantioselective_Direct_Mannich_Reaction_of_Styrylacetates/3394291
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An organocatalyzed direct Mannich reaction of unactivated α-styrylacetates was realized for the first time. By using a quinidine-derived C6′-urea catalyst, the direct Mannich reaction of α-styrylacetates and N-tosylimines gave the desired β-amino esters in high yields, diastereoselectivities, and ee values. The reaction provides a highly stereoselective (up to 96:4 dr and 97% ee) and the most straightforward synthesis of functionalized N-tosylated β-amino esters. The products can be used as precursors for the highly selective synthesis of tetrahydrofuran derivatives.
创建时间:
2016-05-27
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