Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81975
Title: Construction of Fused Pyrrolidines and β-Lactones by Carbene-Catalyzed C−N, C−C, and C−O Bond Formations
Authors: Wu, Xingxing
Hao, Lin
Zhang, Yuexia
Rakesh, Maiti
Reddi, Rambabu N.
Yang, Song
Song, Bao-An
Chi, Yonggui Robin
Keywords: Lactones
Heterocycles
Issue Date: 2017
Source: Wu, X., Hao, L., Zhang, Y., Rakesh, M., Reddi, R. N., Yang, S., et al. (2017). Construction of Fused Pyrrolidines and β-Lactones by Carbene-Catalyzed C−N, C−C, and C−O Bond Formations. Angewandte Chemie International Edition, 56(15), 4201-4205.
Series/Report no.: Angewandte Chemie International Edition
Abstract: A carbene-catalyzed intermolecular C−N bond formation, which initiates a highly selective cascade reaction for the synthesis of pyrrolidine fused β-lactones, is disclosed. The nitrogen-containing bicyclic β-lactone products are obtained with good yields and excellent stereoselectivities. Synthetic transformations of the reaction products into useful functional molecules, such as amino catalysts, can be efficiently realized under mild reaction conditions. Mechanistically, this study provides insights into modulating the reactivities of heteroatoms, such as nitrogen atoms, in challenging carbene-catalyzed asymmetric carbon–heteroatom bond-forming reactions.
Description: 5 p.
URI: https://hdl.handle.net/10356/81975
http://hdl.handle.net/10220/42294
ISSN: 1433-7851
DOI: 10.1002/anie.201700045
Schools: School of Physical and Mathematical Sciences 
Rights: © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the author created version of a work that has been peer reviewed and accepted for publication by Angewandte Chemie International Edition, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1002/anie.201700045].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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