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Unprecedented meta-substitution of calixarenes: Direct way to inherently chiral derivatives

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Unprecedented meta-substitution of calixarenes : Direct way to inherently chiral derivatives. / Slavik, Petr; Dudic, Miroslav; Flidrova, Karolina; Sykora, Jan; Cisarova, Ivana; Böhm, Stanislav; Lhotak, Pavel.

In: Organic Letters, Vol. 14, No. 14, 20.07.2012, p. 3628-3631.

Research output: Contribution to journalArticlepeer-review

Harvard

Slavik, P, Dudic, M, Flidrova, K, Sykora, J, Cisarova, I, Böhm, S & Lhotak, P 2012, 'Unprecedented meta-substitution of calixarenes: Direct way to inherently chiral derivatives', Organic Letters, vol. 14, no. 14, pp. 3628-3631. https://doi.org/10.1021/ol301420t

APA

Slavik, P., Dudic, M., Flidrova, K., Sykora, J., Cisarova, I., Böhm, S., & Lhotak, P. (2012). Unprecedented meta-substitution of calixarenes: Direct way to inherently chiral derivatives. Organic Letters, 14(14), 3628-3631. https://doi.org/10.1021/ol301420t

Vancouver

Slavik P, Dudic M, Flidrova K, Sykora J, Cisarova I, Böhm S et al. Unprecedented meta-substitution of calixarenes: Direct way to inherently chiral derivatives. Organic Letters. 2012 Jul 20;14(14):3628-3631. https://doi.org/10.1021/ol301420t

Author

Slavik, Petr ; Dudic, Miroslav ; Flidrova, Karolina ; Sykora, Jan ; Cisarova, Ivana ; Böhm, Stanislav ; Lhotak, Pavel. / Unprecedented meta-substitution of calixarenes : Direct way to inherently chiral derivatives. In: Organic Letters. 2012 ; Vol. 14, No. 14. pp. 3628-3631.

Bibtex - Download

@article{be13f33dca634ac592123085f15993a4,
title = "Unprecedented meta-substitution of calixarenes: Direct way to inherently chiral derivatives",
abstract = "Electrophilic aromatic substitution in the calix[n]arene series is a well-established procedure leading exclusively to para-substituted derivatives. An unprecedented regioselectivity of the mercuration reaction leading to the meta-substituted calix[4]arenes is described. These compounds represent a new type of substitution pattern in classical calixarene chemistry and open the door for the straightforward synthesis of inherently chiral receptors based on calixarenes.",
author = "Petr Slavik and Miroslav Dudic and Karolina Flidrova and Jan Sykora and Ivana Cisarova and Stanislav B{\"o}hm and Pavel Lhotak",
year = "2012",
month = jul,
day = "20",
doi = "10.1021/ol301420t",
language = "English",
volume = "14",
pages = "3628--3631",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "14",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Unprecedented meta-substitution of calixarenes

T2 - Direct way to inherently chiral derivatives

AU - Slavik, Petr

AU - Dudic, Miroslav

AU - Flidrova, Karolina

AU - Sykora, Jan

AU - Cisarova, Ivana

AU - Böhm, Stanislav

AU - Lhotak, Pavel

PY - 2012/7/20

Y1 - 2012/7/20

N2 - Electrophilic aromatic substitution in the calix[n]arene series is a well-established procedure leading exclusively to para-substituted derivatives. An unprecedented regioselectivity of the mercuration reaction leading to the meta-substituted calix[4]arenes is described. These compounds represent a new type of substitution pattern in classical calixarene chemistry and open the door for the straightforward synthesis of inherently chiral receptors based on calixarenes.

AB - Electrophilic aromatic substitution in the calix[n]arene series is a well-established procedure leading exclusively to para-substituted derivatives. An unprecedented regioselectivity of the mercuration reaction leading to the meta-substituted calix[4]arenes is described. These compounds represent a new type of substitution pattern in classical calixarene chemistry and open the door for the straightforward synthesis of inherently chiral receptors based on calixarenes.

UR - http://www.scopus.com/inward/record.url?scp=84864115340&partnerID=8YFLogxK

U2 - 10.1021/ol301420t

DO - 10.1021/ol301420t

M3 - Article

C2 - 22758402

AN - SCOPUS:84864115340

VL - 14

SP - 3628

EP - 3631

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 14

ER -