Symmetry-driven diastereoselective functionalization of simple trianglamine.

Org Biomol Chem

Department of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznańskiego 8, 61-614 Poznań, Poland.

Published: September 2022

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.

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Source
http://dx.doi.org/10.1039/d2ob01226jDOI Listing

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