Zobrazeno 1 - 10
of 291
pro vyhledávání: '"SRN1"'
Akademický článek
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Autor:
Martine Maillard-Boyer, Caroline Castera-Ducros, Pierre Verhaeghe, France Sifredi, Pascal Rathelot, Patrice Vanelle
Publikováno v:
Molecules, Vol 15, Iss 4, Pp 2719-2729 (2010)
A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive SRN1 / ERC1 radical strategy.
Externí odkaz:
https://doaj.org/article/078b25b94c9f4c6db35fd97177b5681b
Publikováno v:
Molecules, Vol 15, Iss 5, Pp 2949-2961 (2010)
New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.
Externí odkaz:
https://doaj.org/article/e2f3fec234d0426b893630184b9f6bcd
Publikováno v:
Molecules, Vol 7, Iss 12, Pp 917-921 (2002)
A convenient route to 3-alkenyl-1-azaanthraquinones via a hetero Diels-Alder reaction between an azadiene and naphthoquinone, a free radical chlorination and an electron transfer reaction is reported.
Externí odkaz:
https://doaj.org/article/242d3c81a68140a4a366263bff1a6d75
Publikováno v:
Molecules, Vol 5, Iss 9, Pp 1068-1079 (2000)
A review on the reactions of triorganyl stannyl ions with haloarenes is presented. Emphasis on the synthetic applications of the resulting triorganyl stannyl aryl compounds is made, with their inherent potential to build large molecules through the S
Externí odkaz:
https://doaj.org/article/ad622dd6f7384c42844d055225977760
Akademický článek
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Publikováno v:
Tetrahedron. 72(48):7875-7887
Under basic conditions aryl halides can undergo SRN1 reactions, BHAS reactions and benzyne formations. Appropriate complex substrates afford an opportunity to study inherent selectivities. SRN1 reactions are usually favoured under photoactivated cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c80a5288657c51b072e6327eb64c776
Autor:
Adouama, Cherif
Le développement de nouvelles méthodologies de synthèse douces et soucieuses de l'environnement apparait de nos jours comme un véritable besoin. Dans ce contexte, la chimie radicalaire permet de réaliser une grande variété de réactions grâce
Externí odkaz:
http://www.theses.fr/2018LYSE1223/document
Photoinduced Synthesis of Dibenzofurans: Intramolecular and Intermolecular Comparative Methodologies
The SRN1 reaction has been used as a powerful tool for the synthesis of heterocycles, and only a few studies about photoinduced intramolecular cyclization to generate a new C-O bond by a radical pathway have been reported. This work introduces two st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc057d6cdca6df905846d687463624a
http://pubs.acs.org/doi/10.1021/acs.joc.8b00742
http://pubs.acs.org/doi/10.1021/acs.joc.8b00742
Autor:
Adouama, Cherif
Publikováno v:
Chimie organique. Université de Lyon, 2018. Français. ⟨NNT : 2018LYSE1223⟩
The development of new, soft and ecofriendly synthetic methodologies is today a real need. In this context, radical Chemistry allows to make a wide diversity of reactions thanks to soft initation steps (electrochemical or photochemical). Tetracyclic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::47a9b9e23225a6501acf86efbd8b810d
https://theses.hal.science/tel-02056844
https://theses.hal.science/tel-02056844