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Synthesis of bis(1,3-dihydroxy-isopropyl)amine by reductive amination of dihydroxyacetone: Open chain equivalent of DMDP and a potential AB4 dendritic monomer

✍ Scribed by David A. Scott; Thomas M. Krülle; Malcolm Finn; Robert J. Nash; Ana L. Winters; Naoki Asano; Terry D. Butters; George W.J. Fleet


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
290 KB
Volume
40
Category
Article
ISSN
0040-4039

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Bis(1,3-dihydroxy-isopropyl)amine (BDI)
✍ David A Scott; Thomas M Krülle; Malcolm Finn; George W.J Fleet 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 145 KB

Bis(1,3-dihydroxy-isopropyl)amine (BDI) 1, a symmetrical AB 4 dendritic building block, is developed into two diamine linkers in which the nitrogen is more nucleophilic. The four primary alcohols in BDI undergo Michael reactions with t-butyl acrylate. Branch cells of this rare multiplicity allow the