立体中心
化学
磷酰胺
环加成
恶唑啉
催化作用
对映选择合成
光学活性
配体(生物化学)
组合化学
立体化学
有机化学
受体
生物化学
寡核苷酸
DNA
作者
Jong‐Un Park,Hye‐In Ahn,Ho-Jun Cho,Zi Xuan,Ju Hyun Kim
标识
DOI:10.1002/adsc.201901497
摘要
Abstract Efficient synthesis of optically active N‐fused 1,3‐oxazolidines containing quaternary and tertiary stereocenters was achieved via Pd‐catalyzed asymmetric (3+2) cycloadditions of sulfamate‐derived cyclic imines and vinylethylene carbonates. Using a chiral phosphoramidite ligand, the cycloadditions proceeded effectively providing sulfamidate‐fused 1,3‐oxazolidines in high yields (up to 96%) with stereoselectivities (up to 25:1 dr; >99% ee). Additionally, the scale‐up reaction and further transformations of the product were also achieved demonstrating the synthetic utility toward the construction of useful heterocycles such as chiral oxazoline bearing a quaternary stereocenter. magnified image
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