Nitration of thiacalix[4]arene derivatives

Tetrahedron Letters

Volumn 43, Issue 41, 2002, Pages 7413-7417

  Lhoták, Pavel ^a   Svoboda Jr , Jiri ^a   Stibor, Ivan ^a   Sykora, Jan ^b  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

^b INSTITUTE OF CHEMICAL PROCESS FUNDAMENTALS   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORINE DERIVATIVE; NITRIC ACID; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SULFONE; SULFUR; THIACALIX[4]ARENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DERIVATIZATION; NITRATION; OXIDATION; REACTION ANALYSIS;

ARENE;

EID: 0037037977     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01667-2     Document Type: Article

References (33)

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27. +.
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30. max=60°). Hydrogen atoms were located from expected geometry and were not refined. Benzene solvent molecule was localised from the difference Fourier map. Carbon atoms in the solvent molecules (both benzene and chloroform) were refined only isotropically and hydrogen atoms were not included. Additionally, carbon atoms of the benzene solvent were restrained in two disordered positions with partial occupancy 0.15. The chloroform molecule was refined with the occupancy 0.5.
31. max=60°). Hydrogen atoms were located from the expected geometry and were not refined. Atoms of the solvent molecule (ethyl acetate) were refined only isotropically and hydrogen atoms were not included both due to the disorder of the solvent into four positions. Crystallographic data for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 185281 and 185282. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK fax: +44 (0) 1223-336033 or e-mail: deposit@ccdc.cam.ac.uk].
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