Diastereoselectively Switchable Enantioselective Trapping of Carbamate Ammonium Ylides with Imines
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文摘
The diastereoselectively switchable enantioselective trapping of protic carbamate ammonium ylides with imines is reported. The intriguing Rh2(OAc)4 and chiral Br酶nsted acid cocatalyzed three-component Mannich-type reaction of a diazo compound, a carbamate, and an imine provides rapid and efficient access to both syn- and anti-伪-substituted 伪,尾-diamino acid derivatives with a high level control of chemo-, diastereo-, and enantioselectivity.

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