Pd-Catalyzed/Ligand-Controlled Regioselective AsymmetricHydrosulfonylation of Alkylallenes or Arylallenes

The metal-catalyzed hydrofunctionalization reaction of allenes is an efficient approach for the construction of new allyl compounds. This work described a palladium-catalyzed/ligand-controlled asymmetric hydrosulfonylation of simple alkylallenes and arylallenes in the presence of Pd<sub>2</sub>dba<sub>3</sub>. Using a Josiphos or Segphos ligand, the alkylallenes or arylallenes could render the corresponding branched chiral allylsulfones with high yields and high enantioselectivities up to 90% and 99% ee, respectively.

Publication Details

Journal
Figshare
Published
2025-02-03
DOI
https://doi.org/10.1021/acs.orglett.4c04259.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Pd-Catalyzed/Ligand-Controlled Regioselective AsymmetricHydrosulfonylation of Alkylallenes or Arylallenes

Figshare
Catalytic C–H Functionalization Methods
article

Pd-Catalyzed/Ligand-Controlled Regioselective AsymmetricHydrosulfonylation of Alkylallenes or Arylallenes

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Abstract

The metal-catalyzed hydrofunctionalization reaction of allenes is an efficient approach for the construction of new allyl compounds. This work described a palladium-catalyzed/ligand-controlled asymmetric hydrosulfonylation of simple alkylallenes and arylallenes in the presence of Pd<sub>2</sub>dba<sub>3</sub>. Using a Josiphos or Segphos ligand, the alkylallenes or arylallenes could render the corresponding branched chiral allylsulfones with high yields and high enantioselectivities up to 90% and 99% ee, respectively.

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Openalex Percentile: Top 58%
Catalytic C–H Functionalization Methods
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Pd-Catalyzed/Ligand-Controlled Regioselective AsymmetricHydrosulfonylation of Alkylallenes or Arylallenes · Figshare (2025) | TGRS Research Map | TGRS