Amino Surface??Functionalized Tris (calix [4] arene) Dendrons with Rigid C3??Symmetric Propeller Cores

…, A Pappalardo, S Pappalardo, MF Parisi

Index: Gattuso, Giuseppe; Grasso, Giulia; Marino, Nino; Notti, Anna; Pappalardo, Andrea; Pappalardo, Sebastiano; Parisi, Melchiorre F. European Journal of Organic Chemistry, 2011 , # 28 p. 5696 - 5703

Full Text: HTML

Citation Number: 3

Abstract

Abstract Dendrons composed of three functionalized cone calix [4] arene substructures covalently bound to rigid C 3-symmetric tris-anilino cores through amide linkages have been obtained by a divergent synthetic protocol involving the coupling of p-nitrocalix [4] arene butanoic acid 9 with tris (4-aminophenyl) amine (TAPA), 1, 3, 5-tris (4-aminophenyl) benzene (TAPB), and 2, 4, 6-tris (4-aminophenyl)-s-triazine (TAPT). Two different ...

Related Articles:

An Enantiomeric Nanoscale Architecture Obtained from a Pseudoenantiomeric Aggregate: Covalent Fixation of Helical Chirality Formed in Self??Assembled Discotic …

[Ishi-I, Tsutomu; Kuwahara, Rempei; Takata, Akihiko; Jeong, Yeonhwan; Sakurai, Kazuo; Mataka, Shuntaro Chemistry - A European Journal, 2006 , vol. 12, # 3 p. 763 - 776]

Synthesis and electrochemical characterization of donor–acceptor phenylazomethine dendrimers

[Tetrahedron Letters, , vol. 46, # 51 p. 8861 - 8864]

More Articles...