Catalyst-Free Dearomative\nAllylboration of Ketones\nwith Benzo[<i>b</i>]thiophenylmethyl Boronic Acids

A novel approach to the dearomative allylboration of\nketones with\nbenzo[<i>b</i>]thiophenylmethyl boronic acids has been developed.\nBy leveraging the inherent reactivity of the boronic acid unit, this\nprocess occurs under mild reaction conditions without the need for\na catalyst, leading to the efficient formation of homoallylic tertiary\nalcohols accompanied by the construction of three-dimensional sulfur-containing\nalicyclic scaffolds in high yields with excellent stereoselectivities.

Publication Details

Journal
Figshare
Published
2024-09-02
DOI
https://doi.org/10.1021/acs.joc.4c01367.s001
Primary Topic
Organoboron and organosilicon chemistry
Type
article
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article

Catalyst-Free Dearomative\nAllylboration of Ketones\nwith Benzo[b]thiophenylmethyl Boronic Acids

Figshare
Organoboron and organosilicon chemistry
article

Catalyst-Free Dearomative\nAllylboration of Ketones\nwith Benzo[b]thiophenylmethyl Boronic Acids

article en

Abstract

A novel approach to the dearomative allylboration of\nketones with\nbenzo[<i>b</i>]thiophenylmethyl boronic acids has been developed.\nBy leveraging the inherent reactivity of the boronic acid unit, this\nprocess occurs under mild reaction conditions without the need for\na catalyst, leading to the efficient formation of homoallylic tertiary\nalcohols accompanied by the construction of three-dimensional sulfur-containing\nalicyclic scaffolds in high yields with excellent stereoselectivities.

Figshare
Openalex Percentile: Top 80%
Organoboron and organosilicon chemistry
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Catalyst-Free Dearomative\nAllylboration of Ketones\nwith Benzo[<i>b</i>]thiophenylmethyl Boronic Acids · Figshare (2024) | TGRS Research Map | TGRS