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|Title:||Highly enantioselective [4 + 2] annulations catalyzed by amino acid-based phosphines: Synthesis of functionalized cyclohexenes and 3-spirocyclohexene-2- oxindoles|
|Citation:||Zhong, F., Han, X., Wang, Y., Lu, Y. (2012-04). Highly enantioselective [4 + 2] annulations catalyzed by amino acid-based phosphines: Synthesis of functionalized cyclohexenes and 3-spirocyclohexene-2- oxindoles. Chemical Science 3 (4) : 1231-1234. ScholarBank@NUS Repository. https://doi.org/10.1039/c2sc00963c|
|Abstract:||Highly enantioselective [4 + 2] annulation of activated alkenes with α-substituted allenoates catalyzed by amino acid-based bifunctional phosphines has been developed for the first time, which provides an easy access to optically enriched functionalized cyclohexenes. In particular, 3-spirocyclohexene-2-oxindoles were prepared in high yields and with excellent enantioselectivities. This journal is © 2012 The Royal Society of Chemistry.|
|Source Title:||Chemical Science|
|Appears in Collections:||Staff Publications|
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