期刊
TETRAHEDRON LETTERS
卷 42, 期 11, 页码 2103-2106出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(00)02345-5
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Oxonaphtoporphyrins show a 1,4 reactivity involving the conjugated pyrrole double bond, the addition being followed by oxidation or elimination leading to rearomatization. Addition of nitrogen or carbon nucleophiles gives amino and substituted aminoporphyrins, or alkyl and cyanoporphyrins, respectively. (C) 2001 Elsevier Science Ltd. All rights reserved.
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