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Showing 1 to 4 of 4 for “"Halolactonization"”.

  1. Design and Synthesis of Enzyme Activated Irreversible Inactivators for Proteases. Suicide Inactivation of Chymotrypsin

    … lactones in modest yields, and a direct halolactonization method which gave the desired halo-enol lactones in very high yields was developed. Several other routes, such as Baeyer-Villiger oxidation of (beta)-halocycloenones and dehydration of (alpha)-haloketone acids were also developed …

    uiuc Repository record for Design and Synthesis of Enzyme Activated Irreversible Inactivators for Proteases. Suicide Inactivation of Chymotrypsin (opens in a new tab)

  2. Halo Enol Lactones as Enzyme-Activated Irreversible Inhibitors of Alpha-Chymotrypsin: I. The Effect of Lactone Substitution Pattern. Ii. Alpha - Amino-Functionalized Lactones

    … were prepared using a halolactonization reaction to convert the appropriate phenyl-substituted acetylenic acid into the corresponding lactone. The 4-phenyl-tetrahydrofuranone and the 5-phenyl-tetrahydropyranone only proved to be competitive inhibitors, and the …

    uiuc Repository record for Halo Enol Lactones as Enzyme-Activated Irreversible Inhibitors of Alpha-Chymotrypsin: I. The Effect of Lactone Substitution Pattern. Ii. Alpha - Amino-Functionalized Lactones (opens in a new tab)

  3. ORGANOCATALYTIC HALOFUNCTIONALIZATION OF OLEFINS

    … produced encouraging enantioselectivty for halolactonization reactions.

    nus Repository record for ORGANOCATALYTIC HALOFUNCTIONALIZATION OF OLEFINS (opens in a new tab)

  4. Selective Synthesis of Trans-fused Lactam-Lactones by Vicinal Difunctionalization of Readily Affordable Allylic Lactams

    <p>With intrinsic versatility and an overwhelming presence in natural products, nitrogen- and oxygen-containing heterocycles boast a plethora of medicinal properties. Specifically, lactams and lactones are the respective luminaries of the antibiotic and flavor worlds. However, the synthesis of …

    central-wash Repository record for Selective Synthesis of Trans-fused Lactam-Lactones by Vicinal Difunctionalization of Readily Affordable Allylic Lactams (opens in a new tab)