New methods to obtain 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation are described. The stereochemistry of the proximal double functionalization reaction is mainly governed by the solvent, the length of the polyether units and the base used to deprotonate the calix[4]arene.

Synthesis of 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation / Arduini, Arturo; Domiano, Laura; Pochini, Andrea; Secchi, Andrea; Ungaro, Rocco; Ugozzoli, Franco; Struck, Oliver; Verboom, Willem; REINHOUDT DAVID, N.. - In: TETRAHEDRON. - ISSN 0040-4020. - 53:(1997), pp. 3767-3776. [10.1016/S0040-4020(97)00097-5]

Synthesis of 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation.

ARDUINI, Arturo;SECCHI, Andrea;
1997-01-01

Abstract

New methods to obtain 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation are described. The stereochemistry of the proximal double functionalization reaction is mainly governed by the solvent, the length of the polyether units and the base used to deprotonate the calix[4]arene.
1997
Synthesis of 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation / Arduini, Arturo; Domiano, Laura; Pochini, Andrea; Secchi, Andrea; Ungaro, Rocco; Ugozzoli, Franco; Struck, Oliver; Verboom, Willem; REINHOUDT DAVID, N.. - In: TETRAHEDRON. - ISSN 0040-4020. - 53:(1997), pp. 3767-3776. [10.1016/S0040-4020(97)00097-5]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/1498531
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