Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/155081
Title: N-Heterocyclic carbene catalyzed aza-benzoin reaction for access to α-aminoketone molecules containing benzothiazole fragments
Authors: Li, Wei
Lv, Jie
Chi, Robin Yonggui
Keywords: Science::Chemistry
Issue Date: 2021
Source: Li, W., Lv, J. & Chi, R. Y. (2021). N-Heterocyclic carbene catalyzed aza-benzoin reaction for access to α-aminoketone molecules containing benzothiazole fragments. Tetrahedron, 94, 132311-. https://dx.doi.org/10.1016/j.tet.2021.132311
Project: NRF-NRFI2016-06
RG108/16
RG5/19
RG1/18
MOE2018-T3-1-003
A1783c0008
A1783c0010
Journal: Tetrahedron
Abstract: An N-Heterocyclic carbene (NHC) catalyzed aza-benzoin reaction of benzothiazole-2-carboxaldehydes and N-sulfonylimines is reported for the first time. The target benzothiazole-containing aminoketone products bearing different substituents and substitution patterns can be obtained in good to excellent yields under mild conditions.
URI: https://hdl.handle.net/10356/155081
ISSN: 0040-4020
DOI: 10.1016/j.tet.2021.132311
Rights: © 2021 Elsevier Ltd. All rights reserved. This paper was published in Tetrahedron and is made available with permission of Elsevier Ltd.
Fulltext Permission: embargo_20230820
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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