Literature DB >> 29105172

Ketenimines Generated from Ynamides: Versatile Building Blocks for Nitrogen-Containing Scaffolds.

Robert H Dodd1, Kevin Cariou1.   

Abstract

Using ynamides as readily available starting materials, a single step can generate highly reactive ketenimines, which can then undergo a variety of transformations. The choice of the method for generating the ketenimine dictates the outcome of the reaction that can, moreover, be precisely steered through minor variations of the starting material. This Concept gives an overview of the different existing methodologies for this objective, showcasing the diverse nitrogen-containing frameworks that can be obtained by this highly versatile strategy.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  building blocks; cycloaddition; ketenimines; rearrangement; ynamides

Year:  2017        PMID: 29105172     DOI: 10.1002/chem.201704689

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

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2.  Copper-catalyzed radical trans-selective hydroboration of ynamides with N-heterocyclic carbene boranes.

Authors:  Kefeng Wang; Qingzhen Yu; Wenli Mao; Yuxin Zheng; Jing Xu; Yukun Wang
Journal:  iScience       Date:  2022-08-17

3.  Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles.

Authors:  Zhenjun Mao; Hao Zeng
Journal:  RSC Adv       Date:  2022-08-31       Impact factor: 4.036

4.  Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure.

Authors:  Guofeng Li; Man Zhao; Junqiu Xie; Ying Yao; Lingyun Mou; Xiaowei Zhang; Xiaomin Guo; Wangsheng Sun; Zheng Wang; Jiecheng Xu; Jianzhong Xue; Tao Hu; Ming Zhang; Min Li; Liang Hong
Journal:  Chem Sci       Date:  2020-03-13       Impact factor: 9.825

  4 in total

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