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Synthesis 2023; 55(12): 1915-1921
DOI: 10.1055/a-2014-3203
DOI: 10.1055/a-2014-3203
paper
Synthesis of Dithioacetals through Iodine-Promoted Insertion Reactions of Vinylsilane to Disulfides and its Application to Diselenoacetalization
We thank the JSPS KAKENHI Grant Number (JP19K05463). Also, this research was partially supported by Ogawa Sho research fund.
Abstract
Described herein is an iodide-promoted insertion reaction of vinyltrimethylsilane into diaryl or dialkyl disulfides in the presence of iodine/KF leading to the production of a 1,1′-adduct, a dithioacetal derivative. This method also accomplishes insertion into a diaryl diselenide to afford the corresponding diselenoacetal derivative.
Key words
disulfide - vinylsilane - iodide molecules - insertion reaction - dithioacetal - diselenoacetalSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2014-3203.
- Supporting Information
Publication History
Received: 29 November 2022
Accepted after revision: 16 January 2023
Accepted Manuscript online:
16 January 2023
Article published online:
09 February 2023
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