Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Bouisseau, A"'
Autor:
Bouisseau, Anais
This thesis documents the development of synthetic methodologies utilising rhodium catalysis for the formation of carbon-carbon bonds and the functionalisation of carbon-sulfur bonds. Chapter 1 provides an overview of the two main areas of research d
Externí odkaz:
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729134
Publikováno v:
In Analytica Chimica Acta 25 March 2014 818:39-45
Autor:
Francesco Venturoni, Jeremy Robertson, Laurent Pellegatti, Marian Lanz, Joerg Sedelmeier, Flavien Susanne, Julien Haber, Patricia Fernandez-Rodriguez, Florian Kleinbeck, Benjamin Martin, Pascale Hoehn, Michael C. Willis, Berthold Schenkel, Sonja Kamptmann, Anaïs Bouisseau
Publikováno v:
Green Chemistry. 19:1439-1448
Hydrogen peroxide embodies an ideal oxidant in terms of atom-economy, availability and green metrics. However, its use has been limited because of risks associated with disproportionation and the exothermic potential of oxidizing reaction mixtures. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa1f3dc9a39eb77547cb99e1ad5d78bd
https://doi.org/10.1039/c6gc02899c
https://doi.org/10.1039/c6gc02899c
Publikováno v:
Chemistry - A European Journal. 10/24/2016, Vol. 22 Issue 44, p15624-15628. 5p.
Autor:
Bouisseau, A
This thesis documents the development of synthetic methodologies utilising rhodium catalysis for the formation of carbon-carbon bonds and the functionalisation of carbon-sulfur bonds. Chapter 1 provides an overview of the two main areas of research d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::7ad91fee2c621febdc219a3f45ce88fb
https://ora.ox.ac.uk/objects/uuid:49d5fa48-b6dd-41bc-97fc-a1f9766f02b8
https://ora.ox.ac.uk/objects/uuid:49d5fa48-b6dd-41bc-97fc-a1f9766f02b8
Publikováno v:
Organic letters. 18(21)
β'-Thio-substituted-enones, assembled from the combination of β-tert-butylthio-substituted aldehydes and alkynes, using rhodium catalysis, are shown to smoothly undergo in situ intramolecular S-conjugate addition to deliver a range of S-heterocycle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f98631ce0b26afbcfee07dd88c75c61
https://pubmed.ncbi.nlm.nih.gov/27779887
https://pubmed.ncbi.nlm.nih.gov/27779887
β’-Thio-substituted-enones, assembled from the combination of β-tert-butylthio-substituted aldehydes and alkynes, using rhodium-catalysis, are shown to smoothly undergo in-situ intramolecular S-conjugate addition to deliver a range of S-heterocyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bf7a2a97e4a8f1aed92a7e44e0ca1432
https://doi.org/10.1021/acs.orglett.6b02909
https://doi.org/10.1021/acs.orglett.6b02909
Publikováno v:
Chemistry: A European Journal. 22(44)
A one-pot three-step sequence involving Rh-catalyzed alkene hydroacylation, sulfide elimination and Rh-catalyzed aryl boronic acid conjugate addition, delivers products of traceless chelation-controlled hydroacylation employing alkyl aldehydes. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d30f5dad26d6172bb563b27b4d9efe45
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A one‐pot three‐step sequence involving Rh‐catalyzed alkene hydroacylation, sulfide elimination and Rh‐catalyzed aryl boronic acid conjugate addition gave products of traceless chelation‐controlled hydroacylation employing alkyl aldehydes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85e5a4d820425cd3bd761bef58a3df1f
https://pubmed.ncbi.nlm.nih.gov/27666437
https://pubmed.ncbi.nlm.nih.gov/27666437
Autor:
Guerin Schneider, Rémi, Bouisseau, Anaïs, Cavelier, Florine, Vialaret, Aurélie, Martinez, Jean
Publikováno v:
France, Patent n° : WO/2015/011230. 2015
The invention relates to a method for the esterification of molecules carrying a polar function, including a step comprising the silylation of the polar groups, and to the use thereof for the quantification of hydroxycinnamoyl-tartaric esters.(FR)Pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::df8b2bbc3ebbfe42cbaae30da4b1802b
https://hal.archives-ouvertes.fr/hal-01122351
https://hal.archives-ouvertes.fr/hal-01122351