Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Morgane Gaydou"'
Autor:
Michael E. Muratore, Francesco Camponovo, Morgane Gaydou, Antonio M. Echavarren, Javier Carreras, Ricarda E. Miller
Publikováno v:
The Journal of Organic Chemistry
A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF6 as a general purpose catalyst. The resulting adducts can be easily converted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0e2466f86973d5fc1b2a85383118438
https://doi.org/10.1021/acs.joc.5b02607
https://doi.org/10.1021/acs.joc.5b02607
Publikováno v:
Journal of the American Chemical Society. 139(35)
A catalytic protocol that reliably predicts and controls the site-selective incorporation of CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8d0ec7964d92148a214a7411a4e7b23
https://pubmed.ncbi.nlm.nih.gov/28814076
https://pubmed.ncbi.nlm.nih.gov/28814076
Publikováno v:
Journal of the American Chemical Society
A catalytic protocol that reliably predicts and controls the site-selective incorporation of CO2 to a wide range of unsaturated hydrocarbons utilizing water as formal hydride source is described. This platform unlocks an opportunity to catalytically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4425beffcd638b18ca8940352acbe5d5
Publikováno v:
Org. Chem. Front.. 1:759-764
The intermolecular gold(i)-catalyzed reactions of propargyl carboxylates, 1,6-enynes, or 7-substituted 1,3,5-cycloheptatrienes with furans afford cyclopentenones, polyenes or polycyclic compounds by related mechanisms initiated by the electrophilic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da4d631ae0edf0916a08e19bef17a03
https://doi.org/10.1039/c4qo00130c
https://doi.org/10.1039/c4qo00130c
Autor:
Antonio M. Echavarren, Morgane Gaydou
Publikováno v:
Angewandte Chemie (International Ed. in English)
Cycloadditions of azides with alkynes to form triazoles under thermal conditions (Huisgen cycloaddition)[1] or in the presence of copper [click reaction, copper-catalyzed azide–alkyne cycloaddition (CuAAC)][2,3] are reactions of fundamental importa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abb1f6f85bbcbd76424a8bb1c2c63847
https://doi.org/10.1002/anie.201308076
https://doi.org/10.1002/anie.201308076
Publikováno v:
ChemInform. 47
A user-friendly Ni-catalyzed reductive carboxylation of benzylic C-N bonds with CO2 is described. This procedure outperforms state-of-the-art techniques for the carboxylation of benzyl electrophiles by avoiding commonly observed parasitic pathways, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d8218f175fe7f3d196a48e3b78b38d4
https://doi.org/10.1002/chin.201636049
https://doi.org/10.1002/chin.201636049
Autor:
Morgane Gaydou, Ricarda E. Miller, Francesco Camponovo, Antonio M. Echavarren, Javier Carreras, Michael E. Muratore
Publikováno v:
ChemInform. 47
A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF6 as a general purpose catalyst. The resulting adducts can be easily converted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1f0a38bf1fe797d7c103e9977b0aa74
https://doi.org/10.1002/chin.201629073
https://doi.org/10.1002/chin.201629073
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
instname
The sustainable utilization of available feedstock materials for preparing valuable compounds holds great promise to revolutionize approaches in organic synthesis. In this regard, the implementation of abundant and inexpensive carbon dioxide (CO2) as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291b962d01254b0845b67925dcc78342
https://pubmed.ncbi.nlm.nih.gov/27573397
https://pubmed.ncbi.nlm.nih.gov/27573397
Publikováno v:
Angewandte Chemie (International ed. in English). 55(16)
A user-friendly Ni-catalyzed reductive carboxylation of benzylic C-N bonds with CO2 is described. This procedure outperforms state-of-the-art techniques for the carboxylation of benzyl electrophiles by avoiding commonly observed parasitic pathways, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62ae4797419f5d77e2f8990fe68e1ca
https://pubmed.ncbi.nlm.nih.gov/26991022
https://pubmed.ncbi.nlm.nih.gov/26991022
Autor:
Pilar Calleja, Óscar Pablo, Morgane Gaydou, Anthony Pitaval, Mihai Raducan, Antonio M. Echavarren, Beatrice Ranieri, Maria João Moreno
Publikováno v:
Chemistry-A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Chemistry (Weinheim an Der Bergstrasse, Germany)
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
1,6-Enynes bearing OR groups at the propargyl position generate α,β-unsaturated gold(I)-carbenes/ gold(I) stabilized allyl cations that can be trapped by alkenes to form cyclopropanes or 1,3-diketones to give products of α-alkylation. The best mig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b480b9f24b1f54b81d0711578936a434