Enantioselective α-chlorination of β-keto esters and amides catalyzed by chiral imidodiphosphoric acids
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DOI: 10.1016/j.tetlet.2018.05.024
Abstract: Abstract Chiral imidodiphosphoric acids were employed as catalysts for the enantioselective α-chlorination of β-keto esters and amides using NCS as the chlorine source, providing a series of optically active products with good to high enantioselectivities… read more here.
Keywords: chiral imidodiphosphoric; chlorination; chlorination keto; enantioselective chlorination ... See more keywords
Chiral Imidodiphosphoric Acid-Catalyzed Highly Diastereo- and Enantioselective Synthesis of Poly-Substituted 3,4-Dihydro-2 H-pyrans: [4 + 2] Cycloadditions of β,γ-Unsaturated α-Ketoesters and 3-Vinylindoles.
Sign Up to like & getrecommendations! Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b01675
Abstract: Imidodiphosphoric acids were employed to catalyze inverse-electron-demand hetero-Diels-Alder reaction of β,γ-unsaturated α-ketoesters and 3-vinylindoles. A series of optically active 3,4-dihydro-2 H-pyran derivatives with three contiguous stereogenic centers was synthesized in excellent yields (70-99%), diastereoselectivities (>20:1),… read more here.
Keywords: ketoesters vinylindoles; imidodiphosphoric acid; catalyzed highly; chiral imidodiphosphoric ... See more keywords