'Amide' presentation slideshows

Derivatives of Carboxylic Acid

Derivatives of Carboxylic Acid. carboxylate. acid chloride. nitrile. acid anhydride. amide. ester. Nomenclature of Acid Halides. IUPAC: alkanoic acid ?? alkanoyl halide Common: alkanic acid ? alkanyl halide. I: 3-aminopropanoyl chloride. I: 4-nitropentanoyl chloride.

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Derivatives of Carboxylic Acid

Derivatives of Carboxylic Acid. carboxylate. acid chloride. nitrile. acid anhydride. amide. ester. Nomenclature of Acid Halides. IUPAC: alkanoic acid ?? alkanoyl halide Common: alkanic acid ? alkanyl halide. I: 3-aminopropanoyl chloride. I: 4-nitropentanoyl chloride.

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COMPARISON OF FTIR SPECTRA OF BIOMOLECULES ACQUIRED USING SYNCHROTRON IR AND THERMAL IR SOURCES

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The C=O stretching frequency

The C=O stretching frequency. aldehydes and ketones. A summary of the principle infrared bands and their assignments. R is an aliphatic group. Aliphatic Aldehyde. Figure IR-14. Butanal, neat liquid, thin film: CH 3 CH 2 CH 2 CHO. Aliphatic Ketone.

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Chapter 12 Functional Groups II and Nomenclature II

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Intramolecular H-bonding Effects on Ion Binding by Aromatic Amides: An Ab Initio Study

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Chapter 2 Structure and Properties of Organic Molecules

Organic Chemistry , L. G. Wade, Jr. Chapter 2 Structure and Properties of Organic Molecules. CH2:4 Hybridization and Molecular Shape. Molecular Shapes. Bond angles cannot be explained with simple s and p orbitals. Use VSEPR theory.

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Lecture 4

Lecture 4. Alkanes Functional Groups Structure and Nomenclature. Organic compounds can be grouped into families by their common structural features We shall survey the nature of the compounds in a tour of the families in this course

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Comparison of intrathecal isobaric bupivacaine-morphine and ropivacaine-morphine for CS delivery

Comparison of intrathecal isobaric bupivacaine-morphine and ropivacaine-morphine for CS delivery Department of Anaesthesiology and Intensive Care and Department of OB&GYN, Facultry of medicine,Selcuk University,Konya,Turkey. BJA 90(5):659-64(2003). BACKGROUND. Ropivacaine A new long acting

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Organic Chemistry Project: Amide

Organic Chemistry Project: Amide. Parisa Jallali Kendal Smith Lindsey Veazie Alyssa Hunt. Basic Structure. Structure: amides have an amino-carbonyl function attached to an alkyl or aromatic group. What is an amide?.

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Amides

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Advanced Medicinal Chemistry

Advanced Medicinal Chemistry. Lecture 3:. Molecular Interactions and Drug Potency. Barrie Martin AstraZeneca R&D Charnwood. Agonists: Measure % Response vs Agonist concentration EC 50 - The agonist concentration that causes 50% of the maximum response. pEC 50 = - log 10 (EC 50 ).

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SULFONAMIDES

SULFONAMIDES. Chapter 19. Lead Compound. Notes Prontosil - red dye Antibacterial activity in vivo (1935) Inactive in vitro Metabolised to active sulfonamide Acts as a prodrug Sulfanilamide - first synthetic antibacterial agent acting on a wide range of infections.

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From dynamics to structure and function of model bio-molecular systems

From dynamics to structure and function of model bio-molecular systems. Presentation by Fabien Fontaine-Vive. &. Thesis supervisors: Mark Johnson ( Institut Laue-Langevin , Grenoble, France ) Gordon Kearley ( University of Technology , Delft ). Defense ceremony, April 24, 2007.

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A one-pot microwave irradiation synthesis of 1,2,4-triazolo[1,5-a]pyrimidines

Synthesis of a series of triazolopyrimidines (4a-j) was achieved from different acetoacetamides, thiophene-2- carbaldehyde and 5-amino-1,2,4-triazole using microwave irradiation within 20-30 minutes with high yield. The structures of the products were supported by FTIR, PMR and mass spectral data.

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Synthesis of some new 1,4-dihydropyrimido[1,2-a]benzimidazoles and evaluation of their biological activity

Synthesis of a series of pyrimido[1,2-a]benzimidazoles (4a-j) was achieved from acetoacetamides, name of aldehyde and benzimidazole using refluxing with DMF and isolated by methanol with high yield and purity. The pyrimido[1,2-a]benzimidazoles of the products were supported by FTIR, PMR and mass spectral data.

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Mode Nomenclature

Mode Nomenclature. Amide I ~80% CO stretch and ~20% CN stretch. Mode Nomenclature. Amide II ~50% NH in plane bend + ~30% CN stretch and ~12% CO in plane bend. Mode Nomenclature. Amide III ~50% NH in plane bend + ~20% CC stretch and ~15% CN in plane bend.

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Wenjun Zhang, 1 Jixun Zhan 1 , Burkhardt I. Wilke, 2 Christopher N. Boddy, 2 * Yi Tang 1 *

An alternate route to phenanthrene and isocoumarin lactones containing polyketides via an amide starter unit. Wenjun Zhang, 1 Jixun Zhan 1 , Burkhardt I. Wilke, 2 Christopher N. Boddy, 2 * Yi Tang 1 *

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