Issue 33, 2017

KOtBu-Catalyzed lithiation of PMDTA and the direct functionalization of bridged alkenes under mild conditions

Abstract

A practical preparation of the reagent PMDTALi using a super base system under mild conditions has been developed. This PMDTALi base has been demonstrated to be a very efficient reagent for the lithiation of bridged alkenes via direct deprotonation. Further reactions with electrophiles and also coupling reactions in the presence of Pd catalysts provide the bridged alkenes with a broad range of functional groups including silyl, alkyl, halogen and aryl substituents. The utilization of this new lithium reagent has brought a new diversity to the choice of lithium reagent for the deprotonation of synthetically challenging systems.

Graphical abstract: KOtBu-Catalyzed lithiation of PMDTA and the direct functionalization of bridged alkenes under mild conditions

Supplementary files

Article information

Article type
Communication
Submitted
16 Mar 2017
Accepted
28 Mar 2017
First published
28 Mar 2017

Chem. Commun., 2017,53, 4589-4592

KOtBu-Catalyzed lithiation of PMDTA and the direct functionalization of bridged alkenes under mild conditions

Y. Wang, J. Liu, L. Huang, R. Zhu, X. Huang, R. Moir and J. Huang, Chem. Commun., 2017, 53, 4589 DOI: 10.1039/C7CC02006F

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