Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Toni Moragas"'
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 12, Pp o3335-o3335 (2010)
The reaction of a sulfur ylide with a chiral non-racemic sulfinyl imine afforded the desired aziridine in excellent yield and subsequent oxidation of the sulfinyl moiety dissolved in anhydrous dichloromethane using a 75% aqueous solution of 3-chlorop
Externí odkaz:
https://doaj.org/article/ed6e04c50a334225985db9a240678003
Publikováno v:
Angewandte Chemie. 130:16178-16214
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4bc35d81e813d911211fbd9d80c4e07
https://doi.org/10.1002/ange.201803186
https://doi.org/10.1002/ange.201803186
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
ACS Catalysis
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
ACS Catalysis
Recercat. Dipósit de la Recerca de Catalunya
instname
The recent years have witnessed the development of metal-catalyzed reductive carboxylation of organic (pseudo)halides with CO2 as C1 source, representing potential powerful alternatives to existing methodologies for preparing carboxylic acids, privil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871bd5d92029e2f5b03b24ea0a3465c4
https://doi.org/10.1021/acscatal.6b02124
https://doi.org/10.1021/acscatal.6b02124
Autor:
William Lewis, Jon-Paul S. Ward, Justine Dutton, Dominika Regentova, Lesley Walton, Robert A. Stockman, José A. Souto, Ian Churcher, Toni Moragas, Ryan M. Liffey
Publikováno v:
Angewandte Chemie International Edition. 55:10047-10051
A novel rearrangement of 2-vinyl aziridine 2-carboxylates to unusual chiral cyclic sulfoximines is described herein. The method allows the synthesis of substituted cyclic sulfoximines in high yields with complete stereocontrol, displaying a wide subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8d36cce421c349733fe4d6d5eae899
https://doi.org/10.1002/anie.201604188
https://doi.org/10.1002/anie.201604188
Publikováno v:
Journal of the American Chemical Society. 138:7504-7507
A catalytic carboxylation of unactivated primary, secondary, and tertiary alkyl chlorides with CO2 at atmospheric pressure is described. This protocol represents the first intermolecular cross-electrophile coupling of unactivated alkyl chlorides, thu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bd2c8d3407c9468475965d3fb7c94cc
https://doi.org/10.1021/jacs.6b04088
https://doi.org/10.1021/jacs.6b04088
Autor:
Ruben Martin, Toni Moragas
Publikováno v:
Synthesis. 48:2816-2822
A nickel-catalyzed reductive carboxylation technique for the synthesis of cyclopropanecarboxylic acids has been developed. This user-friendly and mild transformation operates at atmospheric pressure of carbon dioxide and utilizes either organic halid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cfd0ed5b83d1502a7509069eecffa5f
https://doi.org/10.1055/s-0035-1560439
https://doi.org/10.1055/s-0035-1560439
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:
Nature
Catalytic carbon-carbon bond formation has enabled the streamlining of synthetic routes when assembling complex molecules. It is particularly important when incorporating saturated hydrocarbons, which are common motifs in petrochemicals and biologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35084cf7259e54d1a98f26f6e793c14d
https://pubmed.ncbi.nlm.nih.gov/28470196
https://pubmed.ncbi.nlm.nih.gov/28470196
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:
Journal of the American Chemical Society. 136:17702-17705
A novel Ni-catalyzed regiodivergent reductive carboxylation of allyl esters with CO2 has been developed. This mild, user-friendly, and operationally simple method is characterized by an exquisite selectivity profile that is dictated by the ligand bac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77b4791bb2c311353341bb5f0094e3fd
https://doi.org/10.1021/ja509077a
https://doi.org/10.1021/ja509077a