Search Results - "Pereira, Vera Lúcia Patrocinio"
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Green synthesis of glycerol 1,3-bromo- and iodohydrins under solvent-free conditions
Published in Green chemistry letters and reviews (02-10-2019)“…New eco-friendly conditions for Finkelstein reaction employing homogeneous media or alumina-supported reagents, both solventless, were utilized in the…”
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Diastereoselective synthesis of nitroso acetals from (S,E)-γ-aminated nitroalkenes via multicomponent [4 + 2]/[3 + 2] cycloadditions promoted by LiCl or LiClO4
Published in Beilstein journal of organic chemistry (30-04-2013)“…Chiral nonracemic aminated nitroso acetals were synthesized via diastereoselective multicomponent [4 + 2]/[3 + 2] cycloadditions employing new…”
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Separation of acetins by counter-current chromatography
Published in Journal of separation science (01-05-2011)“…In this work we report the purification of a crude acetin mixture into mono-, di- and triacetin by countercurrent chromatography. The process was initially…”
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A versatile and efficient approach for the synthesis of chiral 1,3-nitroamines and 1,3-diamines via conjugate addition to new (S,E)-γ-aminated nitroalkenes derived from L-α-amino acids
Published in Beilstein journal of organic chemistry (30-04-2013)“…New chiral (S,E)-γ-N,N-dibenzylated nitroalkenes 2a-c were synthesized from natural L-(α)-amino acids in five steps with overall yields of 68-88%. The…”
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Obtaining glycerol alkyl ethers via Williamson synthesis in heterogeneous media using amberlyst-A26TM −OH form and KOH/Al2O3 as basic solid reagents
Published in Green chemistry letters and reviews (01-12-2024)“…Two innovative and efficient routes were developed to produce glycerol-alkyl ethers employing Williamson reaction conditions in a heterogeneous medium. Thus,…”
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Diastereoselective synthesis of nitroso acetals from ( S , E )-γ-aminated nitroalkenes via multicomponent [4 + 2]/[3 + 2] cycloadditions promoted by LiCl or LiClO 4
Published in Beilstein journal of organic chemistry (30-04-2013)“…Chiral nonracemic aminated nitroso acetals were synthesized via diastereoselective multicomponent [4 + 2]/[3 + 2] cycloadditions employing new ( S , E…”
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Journal Article