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Lecture #13 – Introduction to Amino Acids and Proteins
Lecture #13 – Introduction to Amino Acids and Proteins

... (ex: monosaccharides, alcohols, fatty acids, amino acids) 1) General structure and functional groups 2) Polar and non-polar portions 3) Hydrogen bonding capabilities 4) Acid-Base properties 5) Optical activity 6) Other chemical properties ...
PPT file
PPT file

... Because electrophilic addition to a carbonyl group is reactantfavoured, whenever we see a gem-diol (two –OH groups on one carbon) or a carbon atom with a –OH group and a halogen attached, we expect it to collapse to a carbonyl group: H O C ...
Chapter 23 Functional Groups
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...  Derivatives of the carboxylic acids, in which the -OH from the carboxyl group is replaced by an -OR from an alcohol: carboxylic acid + alcohol  ester + water  many ...
Ch-9-Carboxylic Acids and their derivatives new
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... Carboxylic acids are the most acidic simple organic compounds (they are stronger acids by over ten powers of ten compared to alcohols of comparable weights); also they are more acidic than phenols However, they are weak acids compared to inorganic acids (HCl or H2SO4) Adjacent electron withdrawing s ...
CHAPTER 1 Synthesis of amides using Lewis acid catalyst: Iodine
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... Lewis acids can be drawn. As a common example from the main group elements, AlCl3 finds its application for various purposes.8 One important example is the Friedel‐Crafts alkylation (see scheme 1.3). This reaction, first reported in 1877 by French chemist Charles Friedel and American chemist James C ...
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... phenoxide ion. But alcohols can be converted into sodium alkoxide ion by reaction with sodium metal only. [Alkyl halide used here can not be aryl halide as it does not undergo nucleophilic substitution easily] R – X  can be X = –Cl, –Br, I, (b) ...
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... D. 2 Fe2O3 (s) + 3 C (s) + heat  4 Fe (s) + 3 CO2 (g) E. C (graphite) + O2 (g)  CO2 (g) + heat F. CH4 (g) + O2 (g)  CO2 (g) + H2O (l) + heat Question 27 of 28 Based on their descriptions, classify these chemical changes as endothermic or exothermic. A. A chemical change takes place in a container ...
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... 7. Molten iron and carbon monoxide are produced in a blast furnace by the reaction of iron(III) oxide and coke (pure carbon). If 25.0 kilograms of pure Fe2O3 is used, how many kilograms of iron can be produced? The reaction is: Fe2O3 + 3 C ---> 2 Fe + 3 CO 8. The average human requires 120.0 grams o ...
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... are fat-soluble. Your textbook shows structures of all of these types of lipid molecules. Properties of Lipids In this experiment, you will study the solubility of several lipids in water and in a less polar solvent, methylene chloride (CH2Cl2). You will also test several lipids with bromine to dete ...
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what the ribosome is made of tRNA – brings the amino acids to the

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... Domain C: Carbon chemistry Subdomain C2: Other applications of carbon bonds Subdomain C3: The candidate can indicate for a number of carbon bonds which types of reactions they can undergo and which products are then formed. The candidate can: ...
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...  Alcohol fermentation Glucose -> ethanol + carbon dioxide Carboxylic acids Are weak acids Reaction with reactive metals (salts of ethanoic acid are known as ethanoates) Reaction with carbonates Reaction with bases Reaction with alcohols to produce ester and water (esterification) Ester An ester is ...
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A Biocatalytic Henry Reaction-The Hydroxynitrile Lyase from Hevea

... absolute configuration of the product was determined to be S,[5] which is in agreement with the known stereopreference of HbHNL in cyanohydrin reactions. Although the nitroaldol reaction has been known for more than a century,[6] stereoselective protocols started to evolve only a few decades ago. In ...
O R` R
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... Previously we have reported that the enantioselectivity (E) decreased during esterifications of a range of secondary alcohols (1-4) catalyzed by immobilized lipase B from Candida antarctica (Novozym 435) and that addition of enantiopure (R)alcohols, (R)-1, (R)-2, (R)-5, (R)-6 and (R)-7, induced incr ...
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Petasis reaction



The Petasis reaction (alternatively called the Petasis borono–Mannich (PBM) reaction) is the chemical reaction of an amine, aldehyde, and vinyl- or aryl-boronic acid to form substituted amines.Reported in 1993 by Nicos Petasis as a practical method towards the synthesis of a geometrically pure antifungal agent, naftifine, the Petasis reaction can be described as a variation of the Mannich reaction. Rather than generating an enolate to form the substituted amine product, in the Petasis reaction, the vinyl group of the organoboronic acid serves as the nucleophile. In comparison to other methods of generating allyl amines, the Petasis reaction tolerates a multifunctional scaffold, with a variety of amines and organoboronic acids as potential starting materials. Additionally, the reaction does not require anhydrous or inert conditions. As a mild, selective synthesis, the Petasis reaction is useful in generating α-amino acids, and is utilized in combinatorial chemistry and drug discovery.
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