Issue 61, 2019

Synthesis of an enantiopure scorpionate ligand by a nucleophilic addition to a ketenimine and a zinc initiator for the isoselective ROP of rac-lactide

Abstract

A novel nucleophilic addition of an organolithium to a ketenimine to prepare an enantiopure NNN-heteroscorpionate ligand is described. We verified its potential utility as a valuable scaffold for chirality induction through the preparation of enantiopure zinc complexes, which behave as highly efficient initiators to produce highly-enriched isotactic poly(lactide)s (Pi up to 0.88).

Graphical abstract: Synthesis of an enantiopure scorpionate ligand by a nucleophilic addition to a ketenimine and a zinc initiator for the isoselective ROP of rac-lactide

Supplementary files

Article information

Article type
Communication
Submitted
19 Jun 2019
Accepted
02 Jul 2019
First published
02 Jul 2019

Chem. Commun., 2019,55, 8947-8950

Synthesis of an enantiopure scorpionate ligand by a nucleophilic addition to a ketenimine and a zinc initiator for the isoselective ROP of rac-lactide

M. Honrado, S. Sobrino, J. Fernández-Baeza, L. F. Sánchez-Barba, A. Garcés, A. Lara-Sánchez and A. M. Rodríguez, Chem. Commun., 2019, 55, 8947 DOI: 10.1039/C9CC04716F

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