Synthesis of chiral boranes via asymmetric insertion of carbenes into B-H bonds catalyzed by the rhodium(I) diene complex

03 June 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Asymmetric insertion of arydiazoacetates into B-H bonds of NHC-BH2R adducts gives rare compounds with chiral boron centers. The reaction is catalyzed by the rhodium(I) complex with the chiral diene ligand tBu2-TFB, which can be conveniently synthesized by diastereoselective coordination of the racemic diene with (S-Salox)Rh(CO)2. The target boranes were obtained typically in 75−90% yields with 90-95% ee and 2:1-5:1 dr.

Keywords

rhodium
borane
asymmetric catalysis
diazo compounds
carbene insertion

Supplementary materials

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Description
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Supporting information
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Experimental details, copies of NMR spectra, HPLC data, details of DFT calculations
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Optimized structures
Description
XYZ file with structures optimized by DFT calculations
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X-ray structure of 4e'
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X-ray structure of the minor diastereomer of chiral borane 4e'
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