Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles

Rubén Martín; Catharine H. Larsen; Ana Cuenca; Stephen L. Buchwald

doi:10.1021/ol7014225

Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles

Rubén Martín, Catharine H. Larsen, Ana Cuenca, Stephen L. Buchwald

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

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Resum

A highly efficient Cu-catalyzed tandem C-N bond-forming reaction of 1,4-dihalo-1,3-dienes has been developed. The transformation allows the synthesis of pyrroles arid heteroarylpyrroles with a wide variety of functional groups and substitution patterns from readily available precursors.

Idioma original	Anglès
Pàgines (de-a)	3379-3382
Nombre de pàgines	4
Revista	Organic Letters
Volum	9
Número	17
DOIs	https://doi.org/10.1021/ol7014225
Estat de la publicació	Publicada - 16 d’ag. 2007
Publicat externament	Sí

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title = "Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles",

abstract = "A highly efficient Cu-catalyzed tandem C-N bond-forming reaction of 1,4-dihalo-1,3-dienes has been developed. The transformation allows the synthesis of pyrroles arid heteroarylpyrroles with a wide variety of functional groups and substitution patterns from readily available precursors.",

keywords = "Efficient synthesis, Domino reactions, Copper, Cyclization, Chemistry, Derivatives, Ullmann, Amines, Amides",

author = "Rub{\'e}n Mart{\'i}n and Larsen, {Catharine H.} and Ana Cuenca and Buchwald, {Stephen L.}",

year = "2007",

month = aug,

day = "16",

doi = "10.1021/ol7014225",

language = "English",

volume = "9",

pages = "3379--3382",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "17",

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T1 - Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles

AU - Martín, Rubén

AU - Larsen, Catharine H.

AU - Cuenca, Ana

AU - Buchwald, Stephen L.

PY - 2007/8/16

Y1 - 2007/8/16

N2 - A highly efficient Cu-catalyzed tandem C-N bond-forming reaction of 1,4-dihalo-1,3-dienes has been developed. The transformation allows the synthesis of pyrroles arid heteroarylpyrroles with a wide variety of functional groups and substitution patterns from readily available precursors.

AB - A highly efficient Cu-catalyzed tandem C-N bond-forming reaction of 1,4-dihalo-1,3-dienes has been developed. The transformation allows the synthesis of pyrroles arid heteroarylpyrroles with a wide variety of functional groups and substitution patterns from readily available precursors.

KW - Efficient synthesis

KW - Domino reactions

KW - Copper

KW - Cyclization

KW - Chemistry

KW - Derivatives

KW - Ullmann

KW - Amines

KW - Amides

UR - http://www.scopus.com/inward/record.url?scp=34548181107&partnerID=8YFLogxK

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000248658800046&DestLinkType=FullRecord&DestApp=WOS_CPL

U2 - 10.1021/ol7014225

DO - 10.1021/ol7014225

M3 - Article

C2 - 17655316

AN - SCOPUS:34548181107

SN - 1523-7060

VL - 9

SP - 3379

EP - 3382

JO - Organic Letters

JF - Organic Letters

IS - 17

ER -

Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles

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