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^*

^*Autor corresponent d’aquest treball

Producció científica: Article en revista indexada › Article › Avaluat per experts

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Resum

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	Anglès
Pàgines (de-a)	1055-1059
Nombre de pàgines	5
Revista	Journal of Porphyrins and Phthalocyanines
Volum	20
Número	8-11
DOIs	https://doi.org/10.1142/S1088424616500553
Estat de la publicació	Publicada - 1 de nov. 2016

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10.1142/S1088424616500553

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title = "A new synthesis of isoamethyrins: A 4+2 route",

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",

note = "Publisher Copyright: {\textcopyright} 2016 World Scientific Publishing Company.",

year = "2016",

month = nov,

day = "1",

doi = "10.1142/S1088424616500553",

language = "English",

volume = "20",

pages = "1055--1059",

journal = "Journal of Porphyrins and Phthalocyanines",

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TY - JOUR

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

UR - https://www.scopus.com/pages/publications/84981276944

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000390248600019&DestLinkType=FullRecord&DestApp=WOS_CPL

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DO - 10.1142/S1088424616500553

M3 - Article

AN - SCOPUS:84981276944

SN - 1088-4246

VL - 20

SP - 1055

EP - 1059

JO - Journal of Porphyrins and Phthalocyanines

JF - Journal of Porphyrins and Phthalocyanines

IS - 8-11

ER -

A new synthesis of isoamethyrins: A 4+2 route

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