A new synthesis of isoamethyrins: A 4+2 route

Gonzalo Anguera; Salvador Borrós; José I. Borrell; David Sánchez-García

doi:10.1142/S1088424616500553

A new synthesis of isoamethyrins: A 4+2 route

Gonzalo Anguera, Salvador Borrós, José I. Borrell, David Sánchez-García

Producción científica: Artículo en revista indizada › Artículo › revisión exhaustiva

5 Citas (Scopus)

Resumen

A concise and versatile strategy for the preparation of isoamethyrins is presented. The novel procedure is predicated on the acid catalyzed condensation of a quaterpyrrole and a bipyrrole dialdehyde. As application of this procedure an aryl substituted isoamethyrin has been synthetized and characterized.

Idioma original	Inglés
Páginas (desde-hasta)	1055-1059
Número de páginas	5
Publicación	Journal of Porphyrins and Phthalocyanines
Volumen	20
N.º	8-11
DOI	https://doi.org/10.1142/S1088424616500553
Estado	Publicada - 1 nov 2016

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abstract = "A concise and versatile strategy for the preparation of isoamethyrins is presented. The novel procedure is predicated on the acid catalyzed condensation of a quaterpyrrole and a bipyrrole dialdehyde. As application of this procedure an aryl substituted isoamethyrin has been synthetized and characterized.",

keywords = "2,2′-bipyrrole, expanded porphyrins, isoamethyrin, quaterpyrrole",

author = "Gonzalo Anguera and Salvador Borr{\'o}s and Borrell, {Jos{\'e} I.} and David S{\'a}nchez-Garc{\'i}a",

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T1 - A new synthesis of isoamethyrins

T2 - A 4+2 route

AU - Anguera, Gonzalo

AU - Borrós, Salvador

AU - Borrell, José I.

AU - Sánchez-García, David

PY - 2016/11/1

Y1 - 2016/11/1

N2 - A concise and versatile strategy for the preparation of isoamethyrins is presented. The novel procedure is predicated on the acid catalyzed condensation of a quaterpyrrole and a bipyrrole dialdehyde. As application of this procedure an aryl substituted isoamethyrin has been synthetized and characterized.

AB - A concise and versatile strategy for the preparation of isoamethyrins is presented. The novel procedure is predicated on the acid catalyzed condensation of a quaterpyrrole and a bipyrrole dialdehyde. As application of this procedure an aryl substituted isoamethyrin has been synthetized and characterized.

KW - 2,2′-bipyrrole

KW - expanded porphyrins

KW - isoamethyrin

KW - quaterpyrrole

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JO - Journal of Porphyrins and Phthalocyanines

JF - Journal of Porphyrins and Phthalocyanines

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ER -

A new synthesis of isoamethyrins: A 4+2 route

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