Issue 36, 2016, Issue in Progress

Dinuclear zinc-catalyzed desymmetric intramolecular aldolization: an enantioselective construction of spiro[cyclohexanone-oxindole] derivatives

Abstract

Based on oxindole-derived diketones as the substrates, asymmetric desymmetrizing intramolecular aldol or aldol condensation reactions are reported, which are catalyzed by a Trost bis-ProPhenol dinuclear zinc complex. The corresponding spiro[cyclohexanone-oxindole] derivatives were obtained in good yields with moderate to good enantioselectivities.

Graphical abstract: Dinuclear zinc-catalyzed desymmetric intramolecular aldolization: an enantioselective construction of spiro[cyclohexanone-oxindole] derivatives

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2016
Accepted
07 Mar 2016
First published
10 Mar 2016

RSC Adv., 2016,6, 30683-30689

Dinuclear zinc-catalyzed desymmetric intramolecular aldolization: an enantioselective construction of spiro[cyclohexanone-oxindole] derivatives

Y. Zhang, S. Yin, M. Zhao, J. Zhang, H. Li and X. Wang, RSC Adv., 2016, 6, 30683 DOI: 10.1039/C6RA02296K

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