Catalyzed Mizoroki–Heck Reaction or C–H activation

In the last few decades, research on the elaboration by palladium-catalytic processes of C-C bonds or the activation of C–H bonds has increased considerably. Yet there is still room for much improvement in terms of selectivity, or enantioselectivity, via the development of new ligands or the study o...

Description complète

Enregistré dans:
Détails bibliographiques
Auteur principal: Berteina-Raboin, Sabine
Format: Online
Langue:anglais
Publié: MDPI - Multidisciplinary Digital Publishing Institute 2021
Sujets:
Accès en ligne:44751
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
_version_ 1869529401289342976
author Berteina-Raboin, Sabine
author_browse Berteina-Raboin, Sabine
author_facet Berteina-Raboin, Sabine
author_sort Berteina-Raboin, Sabine
collection Directory of Open Access Books
description In the last few decades, research on the elaboration by palladium-catalytic processes of C-C bonds or the activation of C–H bonds has increased considerably. Yet there is still room for much improvement in terms of selectivity, or enantioselectivity, via the development of new ligands or the study of the catalytic effect of other metals to carry out the same chemical transformations. In addition, the attention paid to environmentally friendly methods in terms of the quantities of catalysts, ligands, and solvents is currently indispensable. The Mizoroki-Heck reaction is one of these important catalytic methods which generates C-C bonds in organic synthesis and is also possible by C-H activation. This book, titled “Catalyzed Mizoroki-Heck Reaction or C-H activation” focuses on new advances in the formation of C-C bonds or new C-H activation methods. It contains original research papers and short reviews on the synthesis of biologically active compounds using these catalytic processes, the identification of new catalysts, of new conditions allowing selectivity or enantioselectivity, the activity and stability of catalyst under turnover conditions, and all improvements in catalytic processes.
format Online
id doab-20.500.12854ir-42796
institution Directory of Open Access Books
language eng
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher MDPI - Multidisciplinary Digital Publishing Institute
publisherStr MDPI - Multidisciplinary Digital Publishing Institute
record_format ojs
spelling doab-20.500.12854ir-427962024-04-05T12:33:31Z Catalyzed Mizoroki–Heck Reaction or C–H activation Berteina-Raboin, Sabine QH301-705.5 Q1-390 regioselectivity n/a Pd-catalyzed Heck reaction catalysis dihydrobenzo[c]acridine layered double hydroxide enantioselective C–H activation Mizoroki-Heck reaction C–H activation reviews abscisic acid palladium mechanism Mizoroki-Heck fluorine Henry reaction C-C coupling C–C cross-coupling thienopyrimidines solvent-free alkenes halides thienopyrazines C–C bond formation solid base catalyst C-H activation application cross-coupling alkoxylation thienopyridines Suzuki reaction thema EDItEUR::P Mathematics and Science::PS Biology, life sciences In the last few decades, research on the elaboration by palladium-catalytic processes of C-C bonds or the activation of C–H bonds has increased considerably. Yet there is still room for much improvement in terms of selectivity, or enantioselectivity, via the development of new ligands or the study of the catalytic effect of other metals to carry out the same chemical transformations. In addition, the attention paid to environmentally friendly methods in terms of the quantities of catalysts, ligands, and solvents is currently indispensable. The Mizoroki-Heck reaction is one of these important catalytic methods which generates C-C bonds in organic synthesis and is also possible by C-H activation. This book, titled “Catalyzed Mizoroki-Heck Reaction or C-H activation” focuses on new advances in the formation of C-C bonds or new C-H activation methods. It contains original research papers and short reviews on the synthesis of biologically active compounds using these catalytic processes, the identification of new catalysts, of new conditions allowing selectivity or enantioselectivity, the activity and stability of catalyst under turnover conditions, and all improvements in catalytic processes. 2021-02-11T09:34:47Z 2021-02-11T09:34:47Z 2020-04-07 23:07:08 2020 book 44751 9783039281398 9783039281381 https://directory.doabooks.org/handle/20.500.12854/42796 eng application/octet-stream Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/2026 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-03928-139-8 10.3390/books978-3-03928-139-8 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783039281398 9783039281381 182 open access
spellingShingle QH301-705.5
Q1-390
regioselectivity
n/a
Pd-catalyzed
Heck reaction
catalysis
dihydrobenzo[c]acridine
layered double hydroxide
enantioselective C–H activation
Mizoroki-Heck reaction
C–H activation
reviews
abscisic acid
palladium
mechanism
Mizoroki-Heck
fluorine
Henry reaction
C-C coupling
C–C cross-coupling
thienopyrimidines
solvent-free
alkenes
halides
thienopyrazines
C–C bond formation
solid base catalyst
C-H activation
application
cross-coupling
alkoxylation
thienopyridines
Suzuki reaction
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
Berteina-Raboin, Sabine
Catalyzed Mizoroki–Heck Reaction or C–H activation
title Catalyzed Mizoroki–Heck Reaction or C–H activation
title_full Catalyzed Mizoroki–Heck Reaction or C–H activation
title_fullStr Catalyzed Mizoroki–Heck Reaction or C–H activation
title_full_unstemmed Catalyzed Mizoroki–Heck Reaction or C–H activation
title_short Catalyzed Mizoroki–Heck Reaction or C–H activation
title_sort catalyzed mizoroki heck reaction or c h activation
topic QH301-705.5
Q1-390
regioselectivity
n/a
Pd-catalyzed
Heck reaction
catalysis
dihydrobenzo[c]acridine
layered double hydroxide
enantioselective C–H activation
Mizoroki-Heck reaction
C–H activation
reviews
abscisic acid
palladium
mechanism
Mizoroki-Heck
fluorine
Henry reaction
C-C coupling
C–C cross-coupling
thienopyrimidines
solvent-free
alkenes
halides
thienopyrazines
C–C bond formation
solid base catalyst
C-H activation
application
cross-coupling
alkoxylation
thienopyridines
Suzuki reaction
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
topic_facet QH301-705.5
Q1-390
regioselectivity
n/a
Pd-catalyzed
Heck reaction
catalysis
dihydrobenzo[c]acridine
layered double hydroxide
enantioselective C–H activation
Mizoroki-Heck reaction
C–H activation
reviews
abscisic acid
palladium
mechanism
Mizoroki-Heck
fluorine
Henry reaction
C-C coupling
C–C cross-coupling
thienopyrimidines
solvent-free
alkenes
halides
thienopyrazines
C–C bond formation
solid base catalyst
C-H activation
application
cross-coupling
alkoxylation
thienopyridines
Suzuki reaction
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
url 44751
work_keys_str_mv AT berteinaraboinsabine catalyzedmizorokiheckreactionorchactivation