Scaffold-Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin-3,2′-oxindoles] with Structural Diversity through Catalytic Isatin-Derived 1,3-Dipolar Cycloadditions

Catalytic asymmetric construction of the biologically important spiro[pyrrolidin‐3,2′‐oxindole] scaffold with contiguous quaternary stereogenic centers in excellent stereoselectivities (up to >99:1 d.r., 98 % ee) has been established by using an organocatalytic 1,3‐dipolar cycloaddition of isatin...

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Veröffentlicht in:Chemistry : a European journal 2012-05, Vol.18 (22), p.6885-6894
Hauptverfasser: Shi, Feng, Tao, Zhong-Lin, Luo, Shi-Wei, Tu, Shu-Jiang, Gong, Liu-Zhu
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Sprache:eng
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