3 article(s) from Peñéñory, Alicia B
Selected examples of valuable β-ketosulfides. A: bioactive synthetic compounds, B: natural products....
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Different strategies for the preparation of β-ketosulfides.
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Thiol-free chemoenzymatic synthesis of β-ketosulfides.
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Time-course plot for the CAL-B catalysed hydrolysis of 1a.
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One-pot two-step preparation of phenacylalkylsulfides. aReaction conditions: i. α-haloketone (0.25 ...
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Selective oxidation of the β-ketosulfide 2a.
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Beilstein J. Org. Chem. 2019, 15, 378–387, doi:10.3762/bjoc.15.34
One-pot synthesis of vinyl and alkynyl selenides.
Effect of t-BuOK on the formation of n-octyl alkynyl selenide 5a.
Effect of reactants concentration on alkynyl selenide formation.
Synthesis of N-ethyl-2-(n-octylselanyl)-1H-indole (9) and 3-iodo-2-(n-octylselanyl)benzofuran (10).
Control reactions and mechanistic study.
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Proposed mechanism for the formation of selenides 5.
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Proposed mechanism for the formation of indole 9.
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Beilstein J. Org. Chem. 2017, 13, 910–918, doi:10.3762/bjoc.13.92
Examples of some pharmaceutically and chemically important derivatives.
Synthesis of S-phenyl benzothioate.
Synthesis of S-phenyl thioacetate.
Synthesis of 6 by reaction between 7 and 1.
Reaction of 2-iodobenzoic acid (9) with 1.
Suggested one-pot synthesis of heterocycle 6.
Reaction of N-(2-iodophenyl)acetamide (13) with 1.
Synthesis of 2-methylbenzothiazole (14).
One-pot three-step synthesis of sulfides. (a) KI/I2; (b) BrCH2Ph; (c) MeI; (d) 4-AnI, CuI/1,10-phen...
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Beilstein J. Org. Chem. 2013, 9, 467–475, doi:10.3762/bjoc.9.50
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