Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Schwartz's reagent"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 176-185 (2023)
Dienones are challenging building blocks in natural product synthesis due to their high reactivity and complex synthesis. Based on previous work and own initial results, a new stereospecific sequential hydrozirconation/Pd-catalyzed acylation of enyne
Externí odkaz:
https://doaj.org/article/9d2335f74bd142b897aeea5b095b6961
Autor:
Michał M. Więcław, Bartłomiej Furman
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 115-123 (2021)
Herein we present the direct asymmetric synthesis of tetrazole-functionalized 1-deoxynojirimycin derivatives from simple sugars via a Schwartz’s reagent-mediated reductive amide functionalization followed by a variant of the Ugi–azide multicompon
Externí odkaz:
https://doaj.org/article/dcc4002fc16e4d1f86cf5757f63f3a46
Akademický článek
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Autor:
Mahasoa-Salina Souvenir Zafindrajaona, Jean-Luc Vasse, Alexis Vallée, Aurélien Coelho, Jean-Bernard Behr
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(3)
The diastereoselective access to cyclopentanols and N,O-dimethylcyclopentylhydroxylamines from 4-pentenoic acid-derived Weinreb amides is described. Based on the concomitant generation of both the nucleophilic and the electrophilic poles by hydrozirc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c344cba7ce05be9d277e650a35bed3b
https://pubmed.ncbi.nlm.nih.gov/34797605
https://pubmed.ncbi.nlm.nih.gov/34797605
Publikováno v:
Polymer. 170:24-30
The carbon-carbon double bonds (C C) in polychloroprene (PCP) was broken down by Schwartz's reagent ([Cp2ZrClH]n) under mild conditions. The reaction mechanism for cleaving C C bonds in PCP was studied in detail. It was found that the cleavage pathwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8ca44044469f591a5502ed2ee3b21d1
https://doi.org/10.1016/j.polymer.2019.03.007
https://doi.org/10.1016/j.polymer.2019.03.007
Publikováno v:
European Journal of Organic Chemistry. 2018:4828-4844
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::327536b9f25a69e0e50a5acfc486da58
https://doi.org/10.1002/ejoc.201800852
https://doi.org/10.1002/ejoc.201800852
Publikováno v:
European Journal of Organic Chemistry. 2018:6601-6623
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::197211c4bcf5457c324d9eb7b5511bdf
https://doi.org/10.1002/ejoc.201701537
https://doi.org/10.1002/ejoc.201701537
Publikováno v:
The Journal of Organic Chemistry. 82:5981-5985
Highly chemoselective addition of Schwartz's reagent to widely available azlactones is described. This method allows the preparation of challenged functionalized α-amino aldehydes, in good to high isolated yields at room temperature, after only 2 mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c7cf5185ac5da590af1a97ea1116f5
https://doi.org/10.1021/acs.joc.7b00820
https://doi.org/10.1021/acs.joc.7b00820
Akademický článek
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Autor:
Artur Ulikowski, Bartłomiej Furman
Publikováno v:
Organic Letters. 18:149-151
An expeditious, functional group-tolerant synthesis of indoles from isatins is described. Isatins are treated with Grignard reagents to yield oxindoles. These, in turn, are reduced with Schwartz's reagent and subjected to nucleophile addition and deh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0abaa58af06a749cc83ff4249f9af8d2
https://doi.org/10.1021/acs.orglett.5b03449
https://doi.org/10.1021/acs.orglett.5b03449