Bu4NF-BF3·Et2O as a new reagent for the selective deprotection of the enol ethers of γ-alkoxyallylstananes

Vladimir Gevorgyan; Yoshinori Yamamoto

doi:10.1039/C39940000059

Bu₄NF-BF₃·Et₂O as a new reagent for the selective deprotection of the enol ethers of γ-alkoxyallylstananes

Vladimir Gevorgyan, Yoshinori Yamamoto

Research output: Contribution to journal › Article

7 Scopus citations

Abstract

The combination of Bu₄NF-BF₃·OEt₂ deprotects selectively the enol ether protecting group of γ-alkoxy- and benzyloxy-allytributylstannanes, without destannylating the tributylstannyl group, affording the corresponding γ-tributylstannyl aldehyde in high yield.

Original language	English (US)
Pages (from-to)	59-60
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	1
DOIs	https://doi.org/10.1039/C39940000059
State	Published - Dec 1 1994
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

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Gevorgyan, V., & Yamamoto, Y. (1994). Bu₄NF-BF₃·Et₂O as a new reagent for the selective deprotection of the enol ethers of γ-alkoxyallylstananes. Journal of the Chemical Society, Chemical Communications, (1), 59-60. https://doi.org/10.1039/C39940000059

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abstract = "The combination of Bu4NF-BF3·OEt2 deprotects selectively the enol ether protecting group of γ-alkoxy- and benzyloxy-allytributylstannanes, without destannylating the tributylstannyl group, affording the corresponding γ-tributylstannyl aldehyde in high yield.",

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