Issue 17, 2019

Dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction: synthesis of 1,2,3-trisubstituted indanes bearing phosphoryl groups

Abstract

A new dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction of o-dienones and dialkyl phosphates is reported. This method has been proven to be general and efficient for the formation of a range of chiral 1,2,3-trisubstituted indane compounds containing phosphorus groups in good yields (up to 92%) with excellent stereoselectivities (up to >99% ee and up to >99 : 1 dr). The relative configuration of the product was identified as having a trans,trans substitution pattern via two-dimensional (2D) nuclear Overhauser effect spectroscopy 1H–1H NMR experiments. A possible mechanism was proposed.

Graphical abstract: Dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction: synthesis of 1,2,3-trisubstituted indanes bearing phosphoryl groups

Supplementary files

Article information

Article type
Paper
Submitted
06 Mar 2019
Accepted
03 Apr 2019
First published
03 Apr 2019

Org. Biomol. Chem., 2019,17, 4301-4310

Dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction: synthesis of 1,2,3-trisubstituted indanes bearing phosphoryl groups

B. Tao, H. Yang, Y. Hua and M. Wang, Org. Biomol. Chem., 2019, 17, 4301 DOI: 10.1039/C9OB00544G

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