Issue 19, 2021

Studies on a catalytic version of the Matteson asymmetric homologation reaction

Abstract

Studies of a catalytic asymmetric version of the Matteson reaction between dichloromethylboronates and organolithium reagents have been undertaken. From several different chiral catalytic systems studied, only one based on a mannitol derivative has given substantial asymmetric induction close to that previously achieved with a bis(oxazoline) derivative and ytterbium triflate. More detailed study of the latter reaction revealed that fresh ytterbium triflate actually reduced the level of asymmetric induction, while “aged” ytterbium triflate, or a fresh sample that had been treated with water, brought about improved induction. The implications of these findings are discussed.

Graphical abstract: Studies on a catalytic version of the Matteson asymmetric homologation reaction

Supplementary files

Article information

Article type
Paper
Submitted
29 Mar 2021
Accepted
20 Apr 2021
First published
22 Apr 2021
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2021,19, 4279-4284

Studies on a catalytic version of the Matteson asymmetric homologation reaction

K. Smith, B. A. Saleh, M. B. Alshammari, G. A. El-Hiti and M. C. Elliott, Org. Biomol. Chem., 2021, 19, 4279 DOI: 10.1039/D1OB00604E

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