desymmetrization is reported. The method affords valuable C1-chiral 3-styryl-1,2-dihydroisoquinolines in high yields with excellent enantioselectivities. It is operationally simple and scalable, exhibits broad substrate generality, and is also effective for accessing P-stereogenic cyclic phosphinamides.
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Koner et al. (2026) studied this question.
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