Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103109
Title: One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation
Authors: Xiang, Shaohua
He, Jingxi
Ma, Jimei
Liu, Xue-Wei
Keywords: DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
Issue Date: 2014
Source: Xiang, S., He, J., Ma, J., & Liu, X.-W. (2014). One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation. Chemical communications, 50(32), 4222-4224.
Series/Report no.: Chemical communications
Abstract: A concise and highly efficient strategy for the synthesis of N-glycosyl imidazole analogues is reported. This reaction is based on a palladium catalysed decarboxylative allylation and three steps, namely, carbamation, decarboxylation and allylation are involved. All the substrates can afford the desired products with excellent yields and selectivities.
URI: https://hdl.handle.net/10356/103109
http://hdl.handle.net/10220/24357
DOI: 10.1039/c3cc48041k
Rights: © 2014 The Authors. This is the author created version of a work that has been peer reviewed and accepted for publication in Chemical Communications, published by Royal Society of Chemistry on behalf of The Authors. 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: [Article DOI: http://dx.doi.org/10.1039/c3cc48041k].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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