Synthesis of biaryls via palladium-catalyzed cross-coupling reactions

Synthesis of biaryls via palladium-catalyzed cross-coupling reactions

The biaryl moiety, a molecular structure commonly encountered in organic chemistry, is present in many natural products or synthetic substances of biological and pharmaceutical interest.The various modes of obtaining biaryls by palladed catalyzed coupling reactions involving organometallics such a...

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Main Authors: N. LAIDAOUI, H. HADJ-MOKHTAR, D. EL ABED
Format: Article
Language:English
Published: Phytochemistry & Organic Synthesis Laboratory 2018-03-01
Series:PhytoChem & BioSub Journal
Online Access:https://drive.google.com/file/d/1hLoHuj6OruRX80ZgDTbGq3oj9qv-30n-/view?usp=sharing
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spelling doaj-b31f7b23356d4b63921aca425d2e38332020-11-25T02:47:01ZengPhytochemistry & Organic Synthesis LaboratoryPhytoChem & BioSub Journal2170-17682170-17682018-03-01121Synthesis of biaryls via palladium-catalyzed cross-coupling reactionsN. LAIDAOUI 0H. HADJ-MOKHTARD. EL ABED Laboratoire de Chimie Fine, Département de Chimie, Faculté des Sciences Exactes et Appliquées, Université d'Oran 1 Ahmed BenBella, BP. 1524, EL M'naouer, Oran 31100, AlgérieThe biaryl moiety, a molecular structure commonly encountered in organic chemistry, is present in many natural products or synthetic substances of biological and pharmaceutical interest.The various modes of obtaining biaryls by palladed catalyzed coupling reactions involving organometallics such as magnesium (Kumada reaction), zinc (Negishi reaction), tin (Stille reaction), silicon (Hiyama reaction), or boron (Suzuki- Miyaura reaction), and by activation of the aromatic C-H bonds exhibited in this bibliographic study. https://drive.google.com/file/d/1hLoHuj6OruRX80ZgDTbGq3oj9qv-30n-/view?usp=sharing
collection DOAJ
language English
format Article
sources DOAJ
author N. LAIDAOUI
H. HADJ-MOKHTAR
D. EL ABED
spellingShingle N. LAIDAOUI
H. HADJ-MOKHTAR
D. EL ABED
Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
PhytoChem & BioSub Journal
author_facet N. LAIDAOUI
H. HADJ-MOKHTAR
D. EL ABED
author_sort N. LAIDAOUI
title Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
title_short Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
title_full Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
title_fullStr Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
title_full_unstemmed Synthesis of biaryls via palladium-catalyzed cross-coupling reactions
title_sort synthesis of biaryls via palladium-catalyzed cross-coupling reactions
publisher Phytochemistry & Organic Synthesis Laboratory
series PhytoChem & BioSub Journal
issn 2170-1768
2170-1768
publishDate 2018-03-01
description The biaryl moiety, a molecular structure commonly encountered in organic chemistry, is present in many natural products or synthetic substances of biological and pharmaceutical interest.The various modes of obtaining biaryls by palladed catalyzed coupling reactions involving organometallics such as magnesium (Kumada reaction), zinc (Negishi reaction), tin (Stille reaction), silicon (Hiyama reaction), or boron (Suzuki- Miyaura reaction), and by activation of the aromatic C-H bonds exhibited in this bibliographic study.
url https://drive.google.com/file/d/1hLoHuj6OruRX80ZgDTbGq3oj9qv-30n-/view?usp=sharing
work_keys_str_mv AT nlaidaoui synthesisofbiarylsviapalladiumcatalyzedcrosscouplingreactions
AT hhadjmokhtar synthesisofbiarylsviapalladiumcatalyzedcrosscouplingreactions
AT delabed synthesisofbiarylsviapalladiumcatalyzedcrosscouplingreactions
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