Issue 43, 2021

Diastereodivergent synthesis of 4-oxocyclohexanecarbaldehydes by using the modularly designed organocatalysts upon switching on their iminium catalysis

Abstract

The cinchona thiourea moiety in the self-assembled modularly designed organocatalysts (MDOs) switches off the iminium catalysis of these catalysts. In this study, it was found that the inhibited iminium catalysis could be switched on by using an appropriate weak acid and that, once the iminium catalysis was switched on, these catalysts could be applied for the highly stereoselective and diastereodivergent synthesis of 4-oxocyclohexanecarbaldehydes via a domino reaction between ketones and α,β-unsaturated aldehydes.

Graphical abstract: Diastereodivergent synthesis of 4-oxocyclohexanecarbaldehydes by using the modularly designed organocatalysts upon switching on their iminium catalysis

Supplementary files

Article information

Article type
Communication
Submitted
23 Feb 2021
Accepted
25 Apr 2021
First published
27 Apr 2021

Chem. Commun., 2021,57, 5334-5337

Author version available

Diastereodivergent synthesis of 4-oxocyclohexanecarbaldehydes by using the modularly designed organocatalysts upon switching on their iminium catalysis

P. Bora, S. Jakkampudi, R. Parella, N. Sakkani, Q. Dai, M. Bihani, H. D. Arman and J. C.-G. Zhao, Chem. Commun., 2021, 57, 5334 DOI: 10.1039/D1CC01020D

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