Regioselective and efficient halogenation of 4,5-unsubstituted alkyl 3-hydroxypyrrole/3-hydroxythiophene-2-yl-carboxylates-Reference-Cited by-同舟云学术

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Regioselective and efficient halogenation of 4,5-unsubstituted alkyl 3-hydroxypyrrole/3-hydroxythiophene-2-yl-carboxylates

Published:2017-06 Issue:26 Volume:58 Page:2537-2541
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Castillo-Aguilera Omar,Depreux Patrick,Halby Ludovic,Azaroual Nathalie,Arimondo Paola B.,Goossens Laurence

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Importance of heterocyclic chemistry: a review;Arora;Int J Pharm Sci Res,2012

2. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles;Baumann;Beilstein J Org Chem,2013

3. Recent advances in the synthesis of pyrroles by multicomponent reactions;Estévez;Chem Soc Rev,2014

4. Bromination and chlorination of pyrrole and some reactive 1-substituted pyrroles;Gilow;J Org Chem,1981

5. Halogenation of aromatic compounds by N-chloro-, N-bromo-, and N-iodosuccinimide;Tanemura;Chem Lett,2003

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1. Aromatic Substitution;Organic Reaction Mechanisms Series;2020-07-24

2. Design of novel well-defined oligothiophenes bearing donor-acceptor groups (pyrene-porphyrin): Synthesis, characterization, optical properties and energy transfer;Journal of Molecular Structure;2019-05

3. Substrate Controlled Regioselective Bromination of Acylated Pyrroles Using Tetrabutylammonium Tribromide (TBABr3);The Journal of Organic Chemistry;2018-07-03

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