Literature DB >> 12203344

Calix[6]pyrrole and hybrid calix[n]furan[m]pyrroles (n+m=6): syntheses and host-guest chemistry.

Grazia Cafeo1, Franz H Kohnke, Giovanna L La Torre, Melchiorre F Parisi, Rosetta Pistone Nascone, Andrew J P White, David J Williams.   

Abstract

Calix[6]pyrrole 2 and the "hybrid systems" calix[3]furan[3]pyrrole 12, calix[2]furan[4]pyrrole 13, and calix[1]furan[5]pyrrole 14, have been synthesized by increasing conversion of the furan units present in the readily accessible calix[6]furan 3 to pyrroles. The host-guest chemistry of these novel macrocycles towards a number of anions, including halogen ions, dihydrogen phosphate, hydrogen sulfate, nitrate, and cyanide has been investigated in solution by (1)H NMR titration techniques and/or phase transfer experiments. The solid-state structures of the free receptors 2, 12, and 13, the 1:1 complexes of calix[6]pyrrole 2 with chloride and bromide, and the 1:1 complex of 14 with chloride are also reported.

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Year:  2002        PMID: 12203344     DOI: 10.1002/1521-3765(20020715)8:14<3148::AID-CHEM3148>3.0.CO;2-B

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  A calixpyrrole derivative acts as an antagonist to GPER, a G-protein coupled receptor: mechanisms and models.

Authors:  Rosamaria Lappano; Camillo Rosano; Assunta Pisano; Maria Francesca Santolla; Ernestina Marianna De Francesco; Paola De Marco; Vincenza Dolce; Marco Ponassi; Lamberto Felli; Grazia Cafeo; Franz Heinrich Kohnke; Sergio Abonante; Marcello Maggiolini
Journal:  Dis Model Mech       Date:  2015-07-16       Impact factor: 5.758

  1 in total

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