Unknown

Dataset Information

0

Catalytic Hydrodifluoroalkylation of Unactivated Olefins.


ABSTRACT: Herein, we report a modular catalytic technique that streamlines the preparation of gem-difluoroalkanes from unactivated sp3 precursors. The method is characterized by its simplicity, generality, and site selectivity, including the functionalization of advanced intermediates and olefin feedstocks. Our approach is enabled by a cooperative interplay of halogen- and hydrogen-atom transfer, thus offering a new entry point to difluorinated alkyl bioisosteres of interest in drug discovery.

SUBMITTER: Yue WJ 

PROVIDER: S-EPMC9490814 | biostudies-literature | 2022 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Catalytic Hydrodifluoroalkylation of Unactivated Olefins.

Yue Wen-Jun WJ   Day Craig S CS   Brenes Rucinski Adrian J AJ   Martin Ruben R  

Organic letters 20220710 28


Herein, we report a modular catalytic technique that streamlines the preparation of <i>gem</i>-difluoroalkanes from unactivated <i>sp</i><sup>3</sup> precursors. The method is characterized by its simplicity, generality, and site selectivity, including the functionalization of advanced intermediates and olefin feedstocks. Our approach is enabled by a cooperative interplay of halogen- and hydrogen-atom transfer, thus offering a new entry point to difluorinated alkyl bioisosteres of interest in dr  ...[more]

Similar Datasets

| S-EPMC2590937 | biostudies-literature
| S-EPMC5426363 | biostudies-literature
| S-EPMC4490774 | biostudies-literature
| S-EPMC3511869 | biostudies-literature
| S-EPMC3390945 | biostudies-literature
| S-EPMC4852863 | biostudies-literature
| S-EPMC8278970 | biostudies-literature
| S-EPMC9853868 | biostudies-literature
| S-EPMC6677148 | biostudies-literature
| S-EPMC4038264 | biostudies-literature