236349

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Microparticle fabricated from a series of symmetrical lipids based on dihydroxyacetone form textured architectures.

Sara Yazdi et al.

Journal of controlled release : official journal of the Controlled Release Society, 330, 1071-1079 (2020-11-15)

We report the synthesis of a series of symmetrical lipids composed of dihydroxyacetone and even‑carbon fatty acids (eight to sixteen carbons), both components of the human metabolome, and characterize their formulation into porous microparticles through spontaneous emulsification without the use

CHLORINATION OF BUTYRYL CHLORIDE IN THE LIQUID-PHASE.

Korhonen IO.

Acta Chemica Scandinavica. Series B, 35(3), 175-178 (1981)

Palladium-catalyzed Chlorocarbonylation of Aryl (pseudo) Halides through in situ Generation of Carbon Monoxide

Boehm P, et al.

Angewandte Chemie (International Edition in English), 132(41), 18043-18052 (2020)

A lewis acid site-activated reaction in zeolites: thiophene acylation by butyryl chloride.

Isaev Y and Fripiat JJ.

J. Catal., 182(1), 257-263 (1999)

A general method for the synthesis of aryl [11C] methylsulfones: potential PET probes for imaging cyclooxygenase-2 expression

Majo VJ, et al.

Bioorganic & Medicinal Chemistry Letters, 15(19), 4268-4271 (2005)

Free and Immobilized Lecitase™ Ultra as the Biocatalyst in the Kinetic Resolution of (E)-4-Arylbut-3-en-2-yl Esters.

Aleksandra Leśniarek et al.

Molecules (Basel, Switzerland), 25(5) (2020-03-04)

The influence of buffer type, co-solvent type, and acyl chain length was investigated for the enantioselective hydrolysis of racemic 4-arylbut-3-en-2-yl esters using Lecitase™ Ultra (LU). Immobilized preparations of the Lecitase™ Ultra enzyme had significantly higher activity and enantioselectivity than the

Use of multivariate statistical techniques to optimize the separation of 17 capsinoids by ultra performance liquid chromatography using different columns.

Janclei P Coutinho et al.

Talanta, 134, 256-263 (2015-01-27)

In this work a multivariate statistical tool (Derringer and Suich optimization) was proposed for the separation of seventeen capsinoids (natural and synthetic) using the UHPLC-DAD chromatography. Capsinoids were analyzed at 280 nm. The variables optimized were the mobile phase (water

Biotransformations of 2-hydroxy-2-(ethoxyphenylphosphinyl)acetic acid and the determination of the absolute configuration of all isomers.

Paulina Majewska

Bioorganic chemistry, 61, 28-35 (2015-06-13)

2-Hydroxy-2-(ethoxyphenylphosphinyl)acetic acid, a new type of organophosphorus compound possessing two stereogenic centers, was investigated. Racemic 2-butyryloxy-2-(ethoxyphenylphosphinyl)acetic acid was synthesized and hydrolyzed using four bacterial species as biocatalysts. In all cases the reaction was more or less stereoselective and isomers bearing

A Lewis acid site-activated reaction in zeolites: Thiophene acylation by butyryl chloride

Isaev Y and Fripiat JJ

J. Catal., 182(1), 257-263 (1999)

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