ArticleBeilstein journal of organic chemistry2017
Influence of the milling parameters on the nucleophilic substitution reaction of activated β-cyclodextrins.
Article in Beilstein journal of organic chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Comparison of the Conventional and Mechanochemical Syntheses of Cyclodextrin Derivatives.Molecules (Basel, Switzerland) · 2023Review
- From amines to (form)amides: a simple and successful mechanochemical approach.Beilstein journal of organic chemistry · 2022Article
- Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers.Beilstein journal of organic chemistry · 2020Article
- Bromide-assisted chemoselective Heck reaction of 3-bromoindazoles under high-speed ball-milling conditions: synthesis of axitinib.Beilstein journal of organic chemistry · 2018Article
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Authors and funding
6 authors.
Funding
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Abstract
The present work focuses on the mechanochemical preparation of industrially important β-cyclodextrin (CD) derivatives. Activated CDs have been reacted with nitrogen and sulfur nucleophiles using a planetary mill equipped with stainless steel, zirconia and glass milling tools of different sizes. It is shown that the milling frequency and the number as well as the size of the milling balls have an effect on the nucleophilic reaction.
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