Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Karen J. Ardila‐Fierro"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 182-189 (2022)
In the search for versatile reagents compatible with mechanochemical techniques, in this work we studied the reactivity of N-fluorobenzenesulfonimide (NFSI) by ball milling. We corroborated that, by mechanochemistry, NFSI can engage in a variety of r
Externí odkaz:
https://doaj.org/article/49a2626676e649ffbd7af30f97c34cd0
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 811-817 (2019)
In recent times, many biologically relevant building blocks such as amino acids, peptides, saccharides, nucleotides and nucleosides, etc. have been prepared by mechanochemical synthesis. However, mechanosynthesis of lipids by ball milling techniques
Externí odkaz:
https://doaj.org/article/fdbff140409043fa868e30c0b3d7aee9
Publikováno v:
Chemistry methods
Catalyzed reactions of organic substrates that operate continuously by extrusion techniques are rare. In this study, we developed a mechanochemical bromination of unactivated naphthalene (1) with 1, 3-dibromo-5, 5- dimethylhydantoin (DBDMH) catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a067b10d9a4d6529456718a1a0715b
https://doi.org/10.1002/cmtd.202200035
https://doi.org/10.1002/cmtd.202200035
Publikováno v:
ChemSusChem. 14:2145-2162
In recent years, mechanochemistry has been growing into a widely accepted alternative for chemical synthesis. In addition to their efficiency and practicality, mechanochemical reactions are also recognized for their sustainability. The association be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b72356035df25688b3993800c95f323
https://doi.org/10.1002/cssc.202100478
https://doi.org/10.1002/cssc.202100478
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(27)
This work reports the experimentally studied mechanochemical formation of rhodacycles by ball milling pyridine- and quinoline-derived substrates and [Cp*RhCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2582bd4ed75d2f65d3a2f2acd0a8c9dd
https://pubmed.ncbi.nlm.nih.gov/35274769
https://pubmed.ncbi.nlm.nih.gov/35274769
Thisworkreportstheexperimentallystudiedmechanochem ica lformationof rhodacyclesby ballmillingpyridine- andquinoline- derivedsubstratesand[Cp*RhCl2]2inthe presenceof NaOAc.Ex-situanalysisof the mechanochem- icalreactionsusingpowderX-raydiffraction(PXR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45e7aaf21729aacc25cfeeb6bb41dd45
https://www.bib.irb.hr/1190428
https://www.bib.irb.hr/1190428
Publikováno v:
Beilstein journal of organic chemistry
In the search for versatile reagents compatible with mechanochemical techniques, in this work we studied the reactivity of N-fluorobenzenesulfonimide (NFSI) by ball milling. We corroborated that, by mechanochemistry, NFSI can engage in a variety of r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39f33fdd58d263735baf481471cf0cfa
http://fulir.irb.hr/7017/
http://fulir.irb.hr/7017/
Publikováno v:
Beilstein journal of organic chemistry. 18
In the search for versatile reagents compatible with mechanochemical techniques, in this work we studied the reactivity of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cb7f6a2de315bb6a1292d7fae0dc0f3
https://pubmed.ncbi.nlm.nih.gov/35233257
https://pubmed.ncbi.nlm.nih.gov/35233257
Autor:
Martin Etter, Carsten Bolm, Stipe Lukin, Krunoslav Užarević, Ivan Halasz, José G. Hernández, Karen J. Ardila-Fierro
Publikováno v:
Angewandte Chemie / International edition International edition 59(32), 13458-13462 (2020). doi:10.1002/anie.201914921
Angewandte Chemie / International edition International edition 59(32), 13458-13462 (2020). doi:10.1002/anie.201914921
Recent progress in the field of mechanochemistry has expanded the discovery of mechanically induced chemical transformations t
Recent progress in the field of mechanochemistry has expanded the discovery of mechanically induced chemical transformations t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::639e45924c2fababd3597634930ff59a
https://bib-pubdb1.desy.de/record/439032
https://bib-pubdb1.desy.de/record/439032
Publikováno v:
Angewandte Chemie. 130:10878-10882
The ability of mechanochemistry to alter established chemical selectivity is demonstrated. A copper(I)-catalyzed mechanochemical aldehyde/alkyne/amine coupling using calcium carbide as the acetylene source provides selective access to 1,4-diamino-2-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b19d7cee10e508078b3cace32df2b89
https://doi.org/10.1002/ange.201805505
https://doi.org/10.1002/ange.201805505