Zn-Catalyzed Asymmetric Allylation for the Synthesis of Optically Active Allylglycine Derivatives. Regio- and Stereoselective Formal α-Addition of Allylboronates to Hydrazono Esters

We have developed Zn-catalyzed asymmetric allylation of hydrazono esters with allylboronates. The reactions proceeded smoothly in high yields and high stereoselectivities. Remarkably, formal α-addition occurred for α-substituted allylboronates exclusively, and excellent stereoselectivities were obse...

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Veröffentlicht in:Journal of the American Chemical Society 2008-03, Vol.130 (10), p.2914-2915
Hauptverfasser: Fujita, Mari, Nagano, Takashi, Schneider, Uwe, Hamada, Tomoaki, Ogawa, Chikako, Kobayashi, Shū
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Sprache:eng
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Zusammenfassung:We have developed Zn-catalyzed asymmetric allylation of hydrazono esters with allylboronates. The reactions proceeded smoothly in high yields and high stereoselectivities. Remarkably, formal α-addition occurred for α-substituted allylboronates exclusively, and excellent stereoselectivities were observed. This is the first example of catalytic regio- and stereoselective allylations with formal α-addition. In addition, the reaction proceeded in aqueous media, and the use of water is essential. Zn(OH)2 might be a catalyst in this asymmetric allylation, and the catalytic activity of Zn(OH)2 was confirmed. This is also the first case of chiral metal hydroxide-catalyzed asymmetric reactions.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja710627x