Tetraaddition of PhLi to a ketocalixarene derivative

Lev Kuno; Noa Seri; Silvio E. Biali

doi:10.1021/ol070429w

Tetraaddition of PhLi to a ketocalixarene derivative

Lev Kuno, Noa Seri, Silvio E. Biali^*

^*Corresponding author for this work

Institute of Chemistry

Research output: Contribution to journal › Article › peer-review

39 Scopus citations

Abstract

Equation presented Reaction of a ketocatixarene with 2.2 equiv or an excess of PhLi affords diaddition and tetraaddition products, respectively. Ionic hydrogenation of the tetraalcohol 8a yields a calix[4]arene monosubstituted by phenyl groups at all four methylene bridges.

Original language	English
Pages (from-to)	1577-1580
Number of pages	4
Journal	Organic Letters
Volume	9
Issue number	8
DOIs	https://doi.org/10.1021/ol070429w
State	Published - 12 Apr 2007

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title = "Tetraaddition of PhLi to a ketocalixarene derivative",

abstract = "Equation presented Reaction of a ketocatixarene with 2.2 equiv or an excess of PhLi affords diaddition and tetraaddition products, respectively. Ionic hydrogenation of the tetraalcohol 8a yields a calix[4]arene monosubstituted by phenyl groups at all four methylene bridges.",

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AU - Seri, Noa

AU - Biali, Silvio E.

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N2 - Equation presented Reaction of a ketocatixarene with 2.2 equiv or an excess of PhLi affords diaddition and tetraaddition products, respectively. Ionic hydrogenation of the tetraalcohol 8a yields a calix[4]arene monosubstituted by phenyl groups at all four methylene bridges.

AB - Equation presented Reaction of a ketocatixarene with 2.2 equiv or an excess of PhLi affords diaddition and tetraaddition products, respectively. Ionic hydrogenation of the tetraalcohol 8a yields a calix[4]arene monosubstituted by phenyl groups at all four methylene bridges.

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Tetraaddition of PhLi to a ketocalixarene derivative

Abstract

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