Cargando…
The emerging role of radical chemistry in the amination transformation of highly strained [1.1.1]propellane: Bicyclo[1.1.1]pentylamine as bioisosteres of anilines
Bicyclo[1.1.1]pentylamines (BPCAs), emerging as sp(3)-rich surrogates for aniline and its derivatives, demonstrate unique structural features and physicochemical profiles in medicinal and synthetic chemistry. In recent years, compared with conventional synthetic approaches, the rapid development of...
Autores principales: | Pang, Qiwen, Li, Yang, Xie, Xin, Tang, Jie, Liu, Qian, Peng, Cheng, Li, Xiang, Han, Bo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634170/ https://www.ncbi.nlm.nih.gov/pubmed/36339044 http://dx.doi.org/10.3389/fchem.2022.997944 |
Ejemplares similares
-
Synthesis of
Sulfur-Substituted Bicyclo[1.1.1]pentanes
by Iodo-Sulfenylation of [1.1.1]Propellane
por: Livesley, Sarah, et al.
Publicado: (2022) -
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes
por: Livesley, Sarah, et al.
Publicado: (2021) -
Strain-release 2-azaallyl anion addition/borylation of [1.1.1]propellane: synthesis and functionalization of benzylamine bicyclo[1.1.1]pentyl boronates
por: Shelp, Russell A., et al.
Publicado: (2021) -
Insertion of [1.1.1]propellane into aromatic disulfides
por: Bär, Robin M, et al.
Publicado: (2019) -
Sodium Bicyclo[1.1.1]pentanesulfinate: A Bench‐Stable Precursor for Bicyclo[1.1.1]pentylsulfones and Bicyclo‐ [1.1.1]pentanesulfonamides
por: Bär, Robin M., et al.
Publicado: (2020)