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Published on: February 16, 2020
Metal-Catalyzed Asymmetric Michael Addition in Natural Product Synthesis
Chunngai Hui1, Fan Pu1, Jing Xu1
1Department of Chemistry, South University of Science and Technology of China, No. 1088 Xueyuan Ave., Nanshan District, Shenzhen, Guangdong, 518055, P. R. China.
Abstract:
Asymmetric catalysis for chiral compound synthesis is a rapidly growing field in modern organic chemistry. Asymmetric catalytic processes have been indispensable for the synthesis of enantioselective materials to meet demands from various fields. Michael addition has been used extensively for the construction of C-C bonds under mild conditions. With the discovery and development of organo- and metal-catalyzed asymmetric Michael additions, the synthesis of enantioselective and/or diastereoselective Michael adducts has become possible and increasingly prevalent in the literature. In particular, metal-catalyzed asymmetric Michael addition has been employed as a key reaction in natural product synthesis for the construction of contiguous quaternary stereogenic center(s), which is still a difficult task in organic synthesis. Previously reported applications of metal-catalyzed asymmetric Michael additions in natural product synthesis are presented here and discussed in depth.
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