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Synthesis 2017; 49(21): 4738-4744
DOI: 10.1055/s-0036-1588802
DOI: 10.1055/s-0036-1588802
special topic
Copper(I)-Catalyzed Boryl Substitution of Allyl Aminals: Selective Synthesis of Linear γ-Aminoallylboronates
This study was financially supported by the MEXT (Japan) program (Strategic Molecular and Materials Chemistry through Innovative Coupling Reactions) of Hokkaido University, as well as
Further Information
Publication History
Received: 08 February 2017
Accepted after revision: 30 March 2017
Publication Date:
15 May 2017 (online)

Published as part of the Special Topic Modern Strategies for Borylation in Synthesis
Abstract
A novel approach for the selective synthesis of α-substituted γ-aminoallylboronates through a copper(I)-catalyzed γ-boryl-substitution of allyl aminals is developed. The reaction proceeds with high yield (up to 88%) and good E/Z selectivity (up to >95:5). Subsequent aldehyde allylation using allylboronates affords (Z)-anti-1,2-amino alcohol derivatives with high stereoselectivity (up to 91% yield, and up to 17:83 E/Z).
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0036-1588802.
- Supporting Information
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