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Published in 2022 at "Chirality"
DOI: 10.1002/chir.23478
Abstract: Although the power of chiral sulfinamide reagents in synthetic chemistry has long been recognized, methods for their synthesis are still auxiliary-based approaches which possess the disadvantages of poor atom economy and limited substrate universality. Due…
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Keywords:
chiral nsted;
catalyzed asymmetric;
nsted acid;
acid ... See more keywords
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Published in 2019 at "Journal of Chemical Education"
DOI: 10.1021/acs.jchemed.9b00350
Abstract: Sustainable practices in process chemistry are highlighted by a novel, 9 week team project of 8–12 students, in collaboration with AstraZeneca chemists, in an organic chemistry laboratory. Students synthesize the antiulcer medicine esomeprazole, which involves…
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Keywords:
asymmetric oxidation;
process chemistry;
chemistry;
synthesize antiulcer ... See more keywords
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Published in 2022 at "Chemical communications"
DOI: 10.1039/d1cc06996a
Abstract: The asymmetric oxidation of a sulfur-containing nine-membered heterocycle was achieved for the late-stage introduction of chirality to the substituents of π-electron systems. The oxidation of the sulfur atom considerably influenced the phase-transition behaviour and crystallinity…
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Keywords:
oxidation;
electron systems;
sulfur containing;
late stage ... See more keywords
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Published in 2020 at "Synthetic Communications"
DOI: 10.1080/00397911.2020.1786121
Abstract: Abstract An efficient asymmetric oxidation of sulfides was achieved using (R)-6,6'-dibromo-BINOL as chiral ligand in combination with Ti(OiPr)4 using 70% aqueous tertiary butyl hydroperoxide as oxidant. The resulting sulfoxides had high enantiopurities and good yields.…
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Keywords:
oxidation sulfides;
asymmetric oxidation;
sulfides catalyzed;
dibromo binol ... See more keywords