Incorporation of substituents at the methylene linkages of the calix[5]arene skeleton

Katerina Kogan; Silvio E. Biali

doi:10.1021/jo901450x

Incorporation of substituents at the methylene linkages of the calix[5]arene skeleton

Katerina Kogan
, Silvio E. Biali

Institute of Chemistry

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

20 Scopus citations

Abstract

(Chemical Equation Presented) Under S_N1 reaction conditions, the bromine atoms of the pentabromo p-tert-butylcalix[5]arene 6 were replaced by alkoxy, electron-rich aryl, and acetylacetonate groups.

Original language	English
Pages (from-to)	7172-7175
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	74
Issue number	18
DOIs	https://doi.org/10.1021/jo901450x
State	Published - 18 Sep 2009

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title = "Incorporation of substituents at the methylene linkages of the calix[5]arene skeleton",

abstract = "(Chemical Equation Presented) Under SN1 reaction conditions, the bromine atoms of the pentabromo p-tert-butylcalix[5]arene 6 were replaced by alkoxy, electron-rich aryl, and acetylacetonate groups.",

author = "Katerina Kogan and Biali, \{Silvio E.\}",

year = "2009",

month = sep,

day = "18",

doi = "10.1021/jo901450x",

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T1 - Incorporation of substituents at the methylene linkages of the calix[5]arene skeleton

AU - Kogan, Katerina

AU - Biali, Silvio E.

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N2 - (Chemical Equation Presented) Under SN1 reaction conditions, the bromine atoms of the pentabromo p-tert-butylcalix[5]arene 6 were replaced by alkoxy, electron-rich aryl, and acetylacetonate groups.

AB - (Chemical Equation Presented) Under SN1 reaction conditions, the bromine atoms of the pentabromo p-tert-butylcalix[5]arene 6 were replaced by alkoxy, electron-rich aryl, and acetylacetonate groups.

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JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 18

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Incorporation of substituents at the methylene linkages of the calix[5]arene skeleton

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