Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19928
Title: Reactivity of tetrapyrrolyl nitrones towards dipolarophiles bearing electron-withdrawing groups
Author: da Silva, A. Filipa F.
Barata, Joana F. B.
Silva, Ana M. G.
Neves, M. Graca P. M. S.
Tome, Augusto C.
Silva, Artur M. S.
Cavaleiro, Jose A. S.
Keywords: 1,3-DIPOLAR CYCLOADDITION REACTIONS
ISOXAZOLINE-FUSED CHLORINS
ALKYL NITRILE OXIDES
MESO-TETRAARYLPORPHYRINS
PERIPHERAL FUNCTIONALIZATION
AZOMETHINE YLIDES
PORPHYRINS
BACTERIOCHLORINS
CORROLES
Issue Date: 2015
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Abstract: The reactivity of porphyrinyl and corrolyl nitrones towards dipolarophiles bearing electron-withdrawing groups was studied and it was found that the two nitrones behave differently in 1,3-dipolar cycloaddition reactions. While porphyrinyl nitrone reacts with dimethyl fumarate, dimethyl acetylenedicarboxylate and ethyl propiolate to afford the expected isoxazolidine and isoxazoline cycloadducts, the corrolyl nitrone reacts with dimethyl fumarate to provide an isoxazolidine-substituted corrole but with dimethyl acetylenedicarboxylate it gives amide derivatives. (C) 2015 Elsevier Ltd. All rights reserved.
Peer review: yes
URI: http://hdl.handle.net/10773/19928
DOI: 10.1016/j.tetlet.2015.04.066
ISSN: 0040-4039
Publisher Version: 10.1016/j.tetlet.2015.04.066
Appears in Collections:CICECO - Artigos



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