Issue 17, 2021

A versatile iodo(iii)etherification of terminal ethynylsilanes using BF3–OiPr2 and alkyl benzyl ethers

Abstract

A series of (E)-α-silyl-β-alkoxyvinyl-λ3-iodanes was synthesized from iodosylbenzene, BF3–ether complexes, and terminal ethynylsilanes. The combined use of BF3–OiPr2 and benzyl ethers of primary alcohols (ROBn) allows the chemoselective transfer of primary alkoxy groups (RO) onto the β-position of the terminal ethynylsilanes.

Graphical abstract: A versatile iodo(iii)etherification of terminal ethynylsilanes using BF3–OiPr2 and alkyl benzyl ethers

Supplementary files

Article information

Article type
Communication
Submitted
11 Mar 2021
Accepted
05 Apr 2021
First published
06 Apr 2021

Org. Biomol. Chem., 2021,19, 3825-3828

A versatile iodo(III)etherification of terminal ethynylsilanes using BF3–OiPr2 and alkyl benzyl ethers

T. Matsumoto, H. Hagiyama, K. Kuribayashi, K. Hioki, H. Fujita, M. Ochiai and M. Kunishima, Org. Biomol. Chem., 2021, 19, 3825 DOI: 10.1039/D1OB00479D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements