Issue 34, 2018

Synthesis and application of a new chiral monodentate spiro phosphoramidite ligand based on hexamethyl-1,1′-spirobiindane backbone in asymmetric hydroamination/arylation of alkenes

Abstract

The design and synthesis of a new chiral monodentate spiro phosphoramidite ligand based on a hexamethyl-1,1′-spirobiindane scaffold has been accomplished. The ligand could serve as an elegant chiral monodentate ligand in the Pd-catalyzed asymmetric hydroamination/arylation of alkenes leading to chiral imidazolidin-2-ones with good enantioselectivities.

Graphical abstract: Synthesis and application of a new chiral monodentate spiro phosphoramidite ligand based on hexamethyl-1,1′-spirobiindane backbone in asymmetric hydroamination/arylation of alkenes

Supplementary files

Article information

Article type
Communication
Submitted
25 Jul 2018
Accepted
13 Aug 2018
First published
16 Aug 2018

Org. Biomol. Chem., 2018,16, 6183-6186

Synthesis and application of a new chiral monodentate spiro phosphoramidite ligand based on hexamethyl-1,1′-spirobiindane backbone in asymmetric hydroamination/arylation of alkenes

H. Shan, R. Pan and X. Lin, Org. Biomol. Chem., 2018, 16, 6183 DOI: 10.1039/C8OB01785A

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