Abstract
An efficient procedure for the synthesis of new enantiopure pyrrolidine-based sulfides bearing additional nitrogen donors and secondary amines based on a bicyclic 2-azanorbornane skeleton was developed. Their application as ligands in palladium-catalyzed Tsuji-Trost reactions led to high yields and up to 82% ee. (Chemical Equation Presented).
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Wojaczyńska, E., Kamińska, K., Wojaczyński, J., & Skarzewski, J. (2016). Chiral pyrrolidine thioethers and 2-azanorbornane derivatives bearing additional nitrogen functions. Enantiopure ligands for palladium-catalyzed Tsuji-Trost reaction. Arkivoc, 2017(2), 162–172. https://doi.org/10.3998/ark.5550190.p009.792
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