A conformationally flexible tetrahydroxycalix[4]arene adopting the unusual 1,3-alternate conformation

Noa Seri; Samah Simaan; Mark Botoshansky; Menahem Kaftory; Silvio E. Biali

doi:10.1021/jo034874q

A conformationally flexible tetrahydroxycalix[4]arene adopting the unusual 1,3-alternate conformation

Noa Seri
, Samah Simaan
, Mark Botoshansky
, Menahem Kaftory
, Silvio E. Biali^*

^*Corresponding author for this work

Institute of Chemistry

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

29 Scopus citations

Abstract

The use of a chiral solvating agent enabled the determination of the NMR-silent ring-inversion process of the ketocalixarene 3. Spectroscopic and crystal data indicate that 3 adopts the unusual 1,3-alternate conformation.

Original language	English
Pages (from-to)	7140-7142
Number of pages	3
Journal	Journal of Organic Chemistry
Volume	68
Issue number	18
DOIs	https://doi.org/10.1021/jo034874q
State	Published - 5 Sep 2003

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title = "A conformationally flexible tetrahydroxycalix[4]arene adopting the unusual 1,3-alternate conformation",

abstract = "The use of a chiral solvating agent enabled the determination of the NMR-silent ring-inversion process of the ketocalixarene 3. Spectroscopic and crystal data indicate that 3 adopts the unusual 1,3-alternate conformation.",

author = "Noa Seri and Samah Simaan and Mark Botoshansky and Menahem Kaftory and Biali, \{Silvio E.\}",

year = "2003",

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T1 - A conformationally flexible tetrahydroxycalix[4]arene adopting the unusual 1,3-alternate conformation

AU - Seri, Noa

AU - Simaan, Samah

AU - Botoshansky, Mark

AU - Kaftory, Menahem

AU - Biali, Silvio E.

PY - 2003/9/5

Y1 - 2003/9/5

N2 - The use of a chiral solvating agent enabled the determination of the NMR-silent ring-inversion process of the ketocalixarene 3. Spectroscopic and crystal data indicate that 3 adopts the unusual 1,3-alternate conformation.

AB - The use of a chiral solvating agent enabled the determination of the NMR-silent ring-inversion process of the ketocalixarene 3. Spectroscopic and crystal data indicate that 3 adopts the unusual 1,3-alternate conformation.

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DO - 10.1021/jo034874q

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AN - SCOPUS:0042839397

SN - 0022-3263

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EP - 7142

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 18

ER -

A conformationally flexible tetrahydroxycalix[4]arene adopting the unusual 1,3-alternate conformation

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