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Symmetry-driven diastereoselective functionalization of simple trianglamine†
Paweł Skowronek,Natalia Prusinowska,Mateusz Bardziński,Agnieszka Janiak
Organic & Biomolecular Chemistry Pub Date : 08/25/2022 00:00:00 , DOI:10.1039/D2OB01226J
Abstract

We have found that derivatization of the trianglamine macrocycle by aliphatic aldehydes leads selectively to one of the two possible diastereomeric aminal products. X-ray analysis, NMR measurements and DFT calculations pointed to the product possessing a higher symmetry.

Graphical abstract: Symmetry-driven diastereoselective functionalization of simple trianglamine
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