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amine
amine

Stoichiometry – Chapter 9
Stoichiometry – Chapter 9

... Stoichiometry ? the name given to the study of quantitative relationships that can be derived from formulas and equations. It is from the Greek words stoicheion, meaning ?element? and metron, meaning ?measure?. There are two types: composition stoichiometry (formulas) and reaction stoichiometry ...
Theoretical Competition - Austrian Chemistry Olympiad
Theoretical Competition - Austrian Chemistry Olympiad

... This nucleus will then emit a proton ...
heterogeneous chiral catalyst derived from hydrolyzed
heterogeneous chiral catalyst derived from hydrolyzed

... cumbersome and expensive. However, following the understanding that different enantiomers may have qualitatively distinct physiological effects, [16-20] and instigated by stricter regulations from health authorities, a growing number of new drugs are now marketed as single enantiomers [21-23]. The t ...
T_AllylCF3paperBM[5]
T_AllylCF3paperBM[5]

... to control fluorinated compounds transformations very effectively. CF3-substituted carbocations are very promising but still rare type of fluorinated species exhibited high electrophilicity and selectivity.3 The present work is a continuation of our investigations on electrophilic activation of alke ...
S. Y. B. Sc. Chemistry
S. Y. B. Sc. Chemistry

... Chapter 4 : Aliphatic and Aromatic amines i) Classification and name of amines. ii) Explain physical properties of amine and their derivative. iii) To write and complete various reactions of amines. iv) To explain methods of preparation of amines. v) Distinguish between 1o, 2o, 3o amines. Chapter 5 ...
Chapter 20: Carboxylic Acids and Nitriles
Chapter 20: Carboxylic Acids and Nitriles

... alcohols (The pKa of ethanol is ~16, compared to ~5 for acetic acid)  In an alkoxide ion, the negative charge is localized on oxygen while in a carboxylate ion the negative charge ...
WADE7Lecture10a
WADE7Lecture10a

... • Raney nickel is a hydrogen rich nickel powder that is more reactive than Pd or Pt catalysts. • This reaction is not commonly used because it will also reduce double and triple bonds that may be present in the molecule. • Hydride reagents are more selective so they are used ...
carbohydrates: monosaccharides. oligo
carbohydrates: monosaccharides. oligo

... unbranched chains, so quantity of the isomers is expected to be quite small. However, monosaccharides contain several asymmetric carbon atoms and therefore they show optical isomerism. Thus, aldohexoses have four asymmetric carbon atoms and 16 optical antipodes. They are divided into eight pairs of ...
OS-FGI Lecture2
OS-FGI Lecture2

... Reaction of an alkene with bromine (in a non-polar solvent to discourage ionic reactions) can lead to competing allylic substitution and addition via radical mechanisms: ...
Amines - ncert
Amines - ncert

Ch. 09 Alcohols, Ethers, Epoxides
Ch. 09 Alcohols, Ethers, Epoxides

ENGLISH VERSION Exam Organic Chemistry 2
ENGLISH VERSION Exam Organic Chemistry 2

... Exam Organic Chemistry 2 (KD1100) Wednesday May 21, 2008, 08.00-13.00 Allowed answering aid: molecular models ...
organonitrogen compounds i. amines
organonitrogen compounds i. amines

... of the hydrocarbon grouping. Unfortunately, the term alkylamine is used very commonly in place of alkanamine, while a host of trivial names are used for arenamines. We shall try to indicate both the trivial and the systematic names wnere possible. Some typical amines, their names, and their physical ...
Nomenclature Changes for CA Index Names
Nomenclature Changes for CA Index Names

... cystine > cysteine > alanine > β-alanine > glycine The new rankings attach greater weight to side-chain functional groups. Also, valine outranks the rare isovaline, and cystine is grouped with its reduced form, cysteine, instead of being separated from it by serine. ...
Preparation of Aldehydes and Ketones
Preparation of Aldehydes and Ketones

... Water hydrates the carbonyl group. The addition of water to an aldehyde or ketone is catalyzed by either acid or base. The equilibrium reaction forms geminal diols, also called carbonyl hydrates: ...
Chapter 17 17.1 Biological Functions of Lipids Classification of
Chapter 17 17.1 Biological Functions of Lipids Classification of

RULE
RULE

... H+ addition - step 1, an electrophilic proton is needed to start the reaction H+ removal - step 3, a proton is removed from the protonated alcohol H+ balance? Considering the overall reaction, a proton is not consumed Catalyst - a species that increases the rate of the reaction, but is not consumed ...
Dehydration of alcohols
Dehydration of alcohols

... however, to maintain some pressure and pressures in the from 2 to about 20 carbon atoms per molecule. These ...
Nomenclature
Nomenclature

- Kendriya Vidyalaya NKJ Katni
- Kendriya Vidyalaya NKJ Katni

... 16. Why SO2 is a better reducing agent in alkaline medium as compared to that in acidic medium ? Explain. ...
Elimination Reactions
Elimination Reactions

... entropies than substitutions because eliminations have a greater number of products formed than that of starting compounds). • Any substitution that occurs must take place through an SN1 mechanism ...
lecture 2 - alcohols-ethers
lecture 2 - alcohols-ethers

... organic chemistry. "SN" stands for nucleophilic substitution and the "1" represents the fact that the rate-determining step is unimolecular. ...
HPLC and LC–MS Studies of the Transesterification Reaction of
HPLC and LC–MS Studies of the Transesterification Reaction of

... when isolated individually by fraction collection, could isomerize (convert) reversibly from one to another. A similar isomerization reaction (which involves intramolecular acyl migration on a glucuronic acid ring) has been studied recently by Nicholson and colleagues using LC–NMR (6–11) and also by ...
Aldehydes, Ketones and Carboxylic Acids
Aldehydes, Ketones and Carboxylic Acids

... Aldol condensation is also possible with ketones. Can you now think of a little more complex situation? What will be the products of aldol condensation when two diffrent aldehydes having   hydrogen atoms are used as reactants. In this case, the reaction is called a crossed-aldol condensation. This ...
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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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