A new route to polyurethanes from ethylene carbonate, diamines and diols

By G. Rokicki, A. Piotrowska. 2002

193 citations recorded by the source corpus.

Subfields: Inorganic Chemistry, Molecular Biology, Process Chemistry and Technology

View Paper: https://www.semanticscholar.org/paper/4ae65a2218df92b9d9b0fbdd674153c4b4187eba

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Inorganic Chemistry

1. J. Datta
2. A. Pizzi

In Molecular Biology

1. A. Pizzi

In Process Chemistry and Technology

1. Kamila Błażek
2. J. Datta
3. A. Pizzi

Citations in the corpus

• Renewable natural resources as green alternative substrates to obtain bio-based non-isocyanate polyurethanes-review (2019, background): “…to the reaction between di- or polycarbamates and diols (Unverferth, Kreye, Prohammer, & Meier, 2013), di- or polycarbonates and amino alcohols (Rokicki & Piotrowska, 2002) or diamines (Ochiai & Utsuno, 2013; Ubaghs, Fricke, Keul, & H€ocker, 2004), polychloroformate and polyamine as well as…”
• Wood products and green chemistry (2016, background): “Routes to obtain polyurethanes without isocyanates exist, by using cyclic carbonate groups and diamines, but amazingly, these have been used with synthetic and not natural polyols (Rokicki and Piotrowska 2002; Nohra et al. 2013).”