Zobrazeno 1 - 5 of 5 pro vyhledávání: '"Vittoria Langé"'
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One-Pot Access to 1,7a-Dihydro-1,3a-ethano-indene and 1,8a-Dihydro-1,3a-ethano-azulene Skeletons by a Sequential Gold(I)-Catalyzed Propargyl Claisen Rearrangement/Nazarov Cyclization/[4+2] Cycloaddition Reaction
Autor: Vittoria Langé, Dina Scarpi, Antonia Rinaldi, Ernesto G. Occhiato
Publikováno v: The Journal of Organic Chemistry. 85:5078-5086
An efficient synthetic approach to the tricyclic 1,7a-dihydro-1,3a-ethano-indene and 1,8a-dihydro-1,3a-ethano-azulene skeletons from suitable propargyl vinyl ethers is based on a one-pot, multistep process entailing a gold(I)-catalyzed propargyl Clai
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7b1717a13d90757e592c9016c5d458
https://doi.org/10.1021/acs.joc.0c00088
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3
Synthesis of Indenes by the Tandem Gold(I)-Catalyzed Claisen Rearrangement/Hydroarylation Reaction of Propargyl Vinyl Ethers
Autor: Dina Scarpi, Ernesto G. Occhiato, Vittoria Langé, Antonia Rinaldi, Giovanna Zanella, Enrique Gómez-Bengoa
Publikováno v: Addi. Archivo Digital para la Docencia y la Investigación
instname
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
The Journal of Organic Chemistry
The tandem gold(I)-catalyzed propargyl Claisen rearrangement/hydroarylation reaction of suitable propargyl vinyl ethers, followed by in situ reduction of the resulting carbonyl group, provides functionalized indenes in good to excellent yields. The r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b4f886413721d3f63350540366bb62
http://hdl.handle.net/10810/52144
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4
Nanostructured carbon materials decorated with organophosphorus moieties: Synthesis and application
Autor: Alberto Brandi, Maurizio Muniz-Miranda, K. Michał Pietrusiewicz, Giacomo Biagiotti, Vittoria Langé, Anna Flis, Stefano Cicchi, Giacomo Ghini, Cristina Ligi, Stefano Caporali
Publikováno v: Beilstein journal of nanotechnology 8 (2017): 485–493. doi:10.3762/bjnano.8.52
info:cnr-pdr/source/autori:Biagiotti G.; Lange V.; Ligi C.; Caporali S.; Muniz-Miranda M.; Flis A.; Pietrusiewicz K.M.; Ghini G.; Brandi A.; Cicchi S./titolo:Nanostructured carbon materials decorated with organophosphorus moieties: Synthesis and application/doi:10.3762%2Fbjnano.8.52/rivista:Beilstein journal of nanotechnology/anno:2017/pagina_da:485/pagina_a:493/intervallo_pagine:485–493/volume:8
Beilstein Journal of Nanotechnology, Vol 8, Iss 1, Pp 485-493 (2017)
Beilstein Journal of Nanotechnology
A new synthetic approach for the production of carbon nanomaterials (CNM) decorated with organophosphorus moieties is presented. Three different triphenylphosphine oxide (TPPO) derivatives were used to decorate oxidized multiwalled carbon nanotubes (
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef5828e1589d6f7025e2dc0cc5f35734
http://www.scopus.com/inward/record.url?eid=2-s2.0-85014603677&partnerID=q2rCbXpz
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5
Akademický článek
Nanostructured carbon materials decorated with organophosphorus moieties: synthesis and application
Autor: Giacomo Biagiotti, Vittoria Langè, Cristina Ligi, Stefano Caporali, Maurizio Muniz-Miranda, Anna Flis, K. Michał Pietrusiewicz, Giacomo Ghini, Alberto Brandi, Stefano Cicchi
Publikováno v: Beilstein Journal of Nanotechnology, Vol 8, Iss 1, Pp 485-493 (2017)
A new synthetic approach for the production of carbon nanomaterials (CNM) decorated with organophosphorus moieties is presented. Three different triphenylphosphine oxide (TPPO) derivatives were used to decorate oxidized multiwalled carbon nanotubes (
Externí odkaz: https://doaj.org/article/eca7060b6a494d148e4cc2a6a7a5a2a3
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