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"ABSTRACTA series of new 4,5-dihydro-6-oxo-1,2,4-triazino[4,5-b]1,2,3,4-tetrahydro-β-carbolines were synthesized by the reaction of methyl 1,2,3,4-tetrahydro-β-carboline-3-carboxylate and the appropriate hydrazonoyl halide in presence of triethylamine. The structures of the title compounds have been established by their elemental analyses and spectroscopecal data. The microbial features of some of the synthesized compounds were studiedby a known method. "

"This book about perfluoroheteroaromatic chemistry : multifunctional systems from perfluorinated heterocycles by nucleophilic aromatic substitution processes, monofluorinated heterocycles, synthesis of beta-Halofurans, synthesis of halogenated 5- and 6-membered sulfur- and sulfur, nitrogen containing heterocycles, heterocyclic reagents containing nitrogen-halogen bond : recent applications, recent progress on the halogen dance reaction on heterocycles, halogenated heterocycles as pharmaceuticals, sources, occurrence and fate of halogenated heterocyclic pharmaceuticals in the environment, and green methods in halogenation of heterocycles."

"Heterocycles have played a crucial role in the biological and industrial development of society, becoming one of the most researched areas within organic chemistry.The first chapter, is based on microwave theory, the latest developments in instrumentation technology, and the various microwave technologies used for synthesis. The remainder of the chapters are divided into two sections. Section A deals with the five-membered heterocycles (pyrazoles, isoxazoles, triazoles, oxadiazoles, thiazoles, imidazoles, oxazoles, oxazolines etc.) and in Section B, various six-membered heterocycles (triazines, benzoxazoles, benzimidazoles, benzothiazoles) are presented. Both sections contain a detailed, recent literature review of microwave assisted synthesis and its applicability to various aromatic heterocyclics."

"Pada penelitian ini, dilakukan sintesis senyawa ester gliserol asam lemak hasil hidrolisis minyak sawit dan ester gliserol oleat secara enzimatik menggunakan lipase Candida rugosa EC. 3.1.1.3 dalam pelarut n-heksana. Optimasi reaksi dilakukan dengan membuat variasi perbandingan mol antara asam lemak dengan gliserol, yaitu 1:1, 1:2, 1:3, dan 1:4. Hasil persen konversi tertinggi diperoleh dari variasi perbandingan 1:4 sebesar 42 untuk ester gliserol asam lemak hidrolisis minyak sawit dan 58 untuk ester gliserol oleat.Hasil karakterisasi menggunakan FT-IR untuk ester gliserol asam lemak hidrolisis minyak sawit dan ester gliserol oleat menunjukkan adanya puncak serapan gugus C=O ester pada bilangan gelombang 1748 cm-1. Pada ester gliserol asam lemak hidrolisis minyak sawit dan ester gliserol oleat dilakukan uji emulsifier. Tipe emulsi yang terbentuk adalah minyak dalam air o/w . Uji aktivitas antimikroba ester gliserol asam lemak hasil hidrolisis minyak sawit maupun ester gliserol asam oleat ternyta tidak dapat menghambat pertumbuhan Staphylococcus epidermidis dan Propionibacterium acnes.

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Synthesis of glycerol palm oil fatty acid ester and glycerol oleic acid ester were conducted enzymatically using Candida rugosa lipase EC. 3.1.1.3 in n hexane solvent. Optimization of esterification reaction was carried out by varying the mole ratio of fatty acid to glycerol 1 1 1 2 1 3 1 4. The highest conversion percentage was obtained at mole ratio 1 4 with the value of 42 for glycerol palm oil fatty acid ester and 58 for glycerol oleic ester. Esterification products were characterized by FT IR.

The FT IR spectrum showed the ester bond was formed as indicated at 1748 cm 1 for the absorption peak of C O ester group. Both esters were then examined by simple emulsion test and were proved to be an emulsifier. Based on the emulsion test, it was proved that the esterification products have properties as an emulsifier for oil in water o w emulsion type. The antimicrobial activity assay showed that glycerol palm oil fatty acid ester and and glycerol oleic acid ester cannot inhibit the growth of Staphylococcus epidermidis and Propionibacterium acnes."