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March 3, 20260 citationsOpen Access

Dynamic kinetic C(sp2)–Si cross-coupling with Si–B reagents for the atroposelective construction of unsymmetrical heterobiaryls

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YXYao XiaoABAnnika L. BarteltEIElisabeth Irran

Key Points

  • High yields and 99% enantiomeric excess achieved using Pd(acac)2 and CuCl.
  • The method effectively utilizes silylboronic acid esters for diverse functional groups and heterocycles.
  • Transmetalation facilitated by copper enhances both reaction speed and enantioselectivity.
  • Potential for broad application in synthesizing complex organic compounds exists.

Abstract

A dynamic kinetic C(sp2)–Si cross-coupling of heterobiaryl triflates and silylboronic acid esters as silicon pronucleophiles is reported. The deracemization reaction proceeds typically in high yields and with 99% ee when using Pd(acac)2 as the precatalyst and CuCl as a cocatalyst, and (R)-TolBINAP as the chiral ligand. The copper salt assists the transmetalation of the Si–B reagent, thereby accelerating the reaction and also improving enantioselectivity. The method tolerates a wide range of functional groups and heterocycles, and different silyl groups can be introduced.

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Cite This Study

Xiao et al. (2025) studied this question.

synapsesocial.com/papers/69a75b26c6e9836116a21f04https://doi.org/10.14279/depositonce-24669
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