Atroposelective synthesis of N-aryl peptoid atropisomers via a palladium(ii)-catalyzed asymmetric C–H alkynylation strategy. Issue 27 (17th June 2021)

• Record Type: Journal Article
• Authors: Wu, Yong-Jie; Xie, Pei-Pei; Zhou, Gang; Yao, Qi-Jun; Hong, Xin; Shi, Bing-Feng
• Is Part Of: Chemical science. Volume 12:Issue 27(2021)
• Page Start: 9391
• Page End: 9397
• Publication Date: 2021-06-17
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1sc01130h
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : The introduction of chirality into peptoids is an important strategy to determine a discrete and robust secondary structure. Abstract : The introduction of chirality into peptoids is an important strategy to determine a discrete and robust secondary structure. However, the lack of an efficient strategy for the synthesis of structurally diverse chiral peptoids has hampered the studies. Herein, we report the efficient synthesis of a wide variety of N -aryl peptoid atropisomers in good yields with excellent enantioselectivities (up to 99% yield and 99% ee) by palladium-catalyzed asymmetric C–H alkynylation. The inexpensive and commercially available l -pyroglutamic acid was used as an efficient chiral ligand. The exceptional compatibility of the C–H alkynylation with various peptoid oligomers renders this procedure valuable for peptoid modifications. Computational studies suggested that the amino acid ligand distortion controls the enantioselectivity in the Pd/l -pGlu-catalyzed C–H bond activation step.