Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/138239
Title: Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines
Authors: Sun, Jun
Mou, Chengli
Liu, Changyi
Huang, Ruoyan
Zhang, Shupeng
Zheng, Pengcheng
Chi, Robin Yonggui
Keywords: Science::Chemistry::Organic chemistry
Issue Date: 2018
Source: Sun, J., Mou, C., Liu, C., Huang, R., Zhang, S., Zheng, P., & Chi, R. Y. (2018). Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines. Organic Chemistry Frontiers, 5(20), 2992-2996. doi:10.1039/C8QO00877A
Journal: Organic Chemistry Frontiers 
Abstract: A carbene-catalyzed enantioselective cycloaddition reaction between enals and cyclic ketiminophosphonates is disclosed. α-Amino phosphonates bearing sophisticated fused heterocycles and quaternary carbons are afforded with excellent enantioselectivities. The α-amino phosphonate products from our approach exhibit encouraging anti-bacterial activities against X. oryzae pv. oryzae, the bacteria that cause serious diseases to rice and other plants.
URI: https://hdl.handle.net/10356/138239
ISSN: 2052-4110
DOI: 10.1039/C8QO00877A
Schools: School of Physical and Mathematical Sciences 
Rights: © 2018 Partner Organisations. All rights reserved. This paper was published in Organic Chemistry Frontiers and is made available with permission of Partner Organisations.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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