Zobrazeno 1 - 10
of 32
pro vyhledávání: '"C De Lucca"'
Autor:
Eduardo C. S. Rocha, Yasmin N. Salmazo, Marcio Hayashi, César A. D. Zaragoza, Emilio C. de Lucca Júnior
Publikováno v:
Química Nova, Vol 46, Iss 1, Pp 43-76 (2023)
Externí odkaz:
https://doaj.org/article/0b5bea428a7f4a488af03329a592f318
Publikováno v:
Química Nova, Vol 44, Iss 8, Pp 1045-1077 (2021)
MOLECULAR SYMMETRY AND DESYMMETRIZATION REACTIONS IN ORGANIC SYNTHESIS. Molecular Symmetry has found several applications in Organic Chemistry. The aim of this article is to showcase its relevance as a tool for synthetic planning. Natural Products an
Externí odkaz:
https://doaj.org/article/62835d882920435e873a453b15f2a8a5
Autor:
Emilio C. de Lucca Jr, Victor C. S. Santana, Milena C. V. Fernandes, Isadora Cappuccelli, Ana Carolina G. Richieri
Publikováno v:
Synthesis. 54:5337-5359
C–H bond oxidation is a powerful means for oxygen incorporation in organic molecules. Its use results in fast structural diversification and in a new way of thinking about retrosynthetic disconnections. In this review, we present the application of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d58c86cbe56461b4128608dd47c84b5
https://doi.org/10.1055/a-1918-4338
https://doi.org/10.1055/a-1918-4338
Autor:
Victor C. S. Santana, Eduardo C. S. Rocha, Julian C. S. Pavan, Vladimir C. G. Heleno, Emilio C. de Lucca
Publikováno v:
The Journal of Organic Chemistry. 87:10462-10466
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf6e9d8dcc90a88fa42244b56d770b1f
https://doi.org/10.1021/acs.joc.2c01051
https://doi.org/10.1021/acs.joc.2c01051
Publikováno v:
Knowledge Updates 2022/1 ISBN: 9783132451476
This chapter is an update to Science of Synthesis Section 26.1.2, which included the synthesis of ketones by oxidation of alkanes. This contribution is focused on reports published during the period 2007–2020 that describe the synthesis of ketones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eded9621d2faa5f0db3a53591e052385
https://doi.org/10.1055/sos-sd-126-00120
https://doi.org/10.1055/sos-sd-126-00120
Publikováno v:
Nature chemistry
Despite significant progress in the development of site-selective aliphatic C–H oxidations over the past decade, the ability to oxidize strong methylene C–H bonds in the presence of more oxidatively labile aromatic functionalities remains a major
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f28309f01465bae1823c432de3e3487
https://doi.org/10.1038/s41557-018-0175-8
https://doi.org/10.1038/s41557-018-0175-8
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(67)
In this communication, the enantioselective synthesis of phthalides and isochromanones is described through a new palladium-catalyzed Heck-Matsuda arylation/NaBH4 -reduction/lactonization sequence of 2,3- and 2,5-dihydrofurans in good overall yields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d4c8d3158545c2978433b5bfafec235
https://pubmed.ncbi.nlm.nih.gov/30290051
https://pubmed.ncbi.nlm.nih.gov/30290051
Publikováno v:
Journal of the American Chemical Society. 139(41)
Amide-containing molecules are ubiquitous in natural products, pharmaceuticals, and materials science. Due to their intermediate electron-richness, they are not amenable to any of the previously developed N-protection strategies known to enable remot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bddc5e401f2ad02d0a10084d0df9f41b
https://pubmed.ncbi.nlm.nih.gov/28921954
https://pubmed.ncbi.nlm.nih.gov/28921954
Autor:
Sylvie Michel, Ricardo N. dos Santos, Luiz C. Dias, Vanderlan da Silva Bolzani, Wanessa F. Altei, Fernando Cotinguiba, Renan Moraes Pioli, Marilia Valli, Xavier Cachet, Emílio C. de Lucca, Adriano D. Andricopulo, Maysa Furlan, Marco A. Dessoy
Publikováno v:
Journal of the Brazilian Chemical Society v.28 n.3 2017
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Volume: 28, Issue: 3, Pages: 475-484, Published: MAR 2017
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Volume: 28, Issue: 3, Pages: 475-484, Published: MAR 2017
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2018-12-11T17:31:13Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-03-01. Added 1 bitstream(s) on 2019-10-09T18:32:48Z : No. of bitstreams: 1 S0103-50532017000300475.pdf: 612042 bytes, checksum: 72fdf2c23c51d9f3984
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc0fb5ad28b4906a26e1d2ca6bc89ee
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000300475
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000300475