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- Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization. Tassilo Gleede, Louis Reisman, Elisabeth Rieger, Pierre Canisius Mbarushimana, Paul A. Rupar, Frederik R. Wurm
, Polym. Chem.
, 2019
, 10
, 3257
- A new method using compressed CO2 for the in situ functionalization of mesoporous silica with hyperbranched polymers. Pedro López-Aranguren, Lourdes F. Vega, Concepción Domingo
, Chem. Commun.
, 2013
, 49
, 11776
- Solvent and catalyst-free modification of hyperbranched polyethyleneimines by ring-opening-addition or ring-opening-polymerization of N-sulfonyl aziridines. Zhunxuan Li, Rui Chen, Ying Wang, Linlin Zhu, Wenyi Luo, Zhen Zhang, Nikos Hadjichristidis
, Polym. Chem.
, 2021
, 12
, 1787
- Catalyst-free aziridine-based step-growth polymerization: a facile approach to optically active poly(sulfonamide amine)s and poly(sulfonamide dithiocarbamate)s. Shibin Chen, Linlin Zhu, Zhen Zhang
, Polym. Chem.
, 2022
, 13
, 4324
- An overview of porous silica immobilized amines for direct air CO2 capture. Arjun Cherevotan, Jithu Raj, Sebastian C. Peter
, J. Mater. Chem. A
, 2021
, 9
, 27271
- Hybrid aminopolymer–silica materials for efficient CO2 adsorption. Pedro López-Aranguren, Santiago Builes, Julio Fraile, Ana López-Periago, Lourdes F. Vega, Concepción Domingo
, RSC Adv.
, 2015
, 5
, 104943
- Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion. Zhen-Zhen Yang, Liang-Nian He, Jiao Gao, An-Hua Liu, Bing Yu
, Energy Environ. Sci.
, 2012
, 5
, 6602
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Desilylative elimination of the quinazolinone ring from
1-(4-oxoquinazolin-3-yl)-2-silylaziridines; preparation of an N–H
aziridine in high enantiomeric excess by in situ
nucleophilic addition to the derived azirine
. Robert S. Atkinson, Michael P. Coogan, Ian S. T. Lochrie
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 897
- Nucleophilic Reactivity of N-Phosphorylated
Ethyleneimine†. Charlotte Le Roux, Agnes M. Modro, Tomasz A. Modro
, J. Chem. Res. (S)
, 1997
, 100
- Aziridines: epoxides’ ugly cousins?. J. B. Sweeney
, Chem. Soc. Rev.
, 2002
, 31
, 247