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Novel amine-catalysed hydroalkoxylation reactions of
Novel amine-catalysed hydroalkoxylation reactions of

... The importance of b-hydroxycarbonyl compounds and their protected alkoxy analogues in natural product chemistry1 and organic synthesis in general2 is difficult to overstate. While the former class of compounds is readily prepared via (inter alia) the aldol reaction, the direct synthesis of b-alkoxyc ...
Dess-Martin Periodinane
Dess-Martin Periodinane

... One of the mildest reagents for the selective oxidation of primary and secondary alcohols to aldehydes and ketones. High yields can be obtained at ambient temperatures, under neutral conditions, in chloroform, dichloromethane or acetonitrile: J. Org. Chem., 48, 4155 (1983); J. Am. Chem. Soc., 113, 7 ...
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation

... Pyridinium chlorochromate (PCC) reactions are run in anhydrous methylene chloride and the aldehyde cannot form a hydrate z The oxidation of a primary alcohol therefore stops at the ...
Organic Chemistry I Laboratory
Organic Chemistry I Laboratory

... alkenes. Markovnikov discovered that hydrogen iodide adds to propene to form mainly 2-iodopropane. From this and other results, Markovnikov formulated his well-known rule, which can be expressed as follows for a hydrogencontaining species represented by HZ: Markovnikov’s rule: When HZ adds to the ca ...
5-3 - U of L Class Index
5-3 - U of L Class Index

File - Dr KHALID SHADID
File - Dr KHALID SHADID

... • Although acetals are hydrolyzed to aldehydes and kctones in aqueous acid, they are stable in basic solutions. • Because of this property, acetal give a convenient method for protecting aldehyde and ketone groups from undesired reactions in • As an example, let us consider the problem of converting ...
Answers
Answers

Aldehydes and Ketones
Aldehydes and Ketones

... NAMING ALDEHYDES • ALDEHYDES ARE NAMED BY REPLACING THE FINAL “E” OF THE NAME OF THE ALKANE WITH THE SAME NUMBER OF CARBONS TO “AL”. • BECAUSE IN ALDEHYDES THE CARBONYL GROUP IS ALWAYS ATTACHED TO THE FIRST CARBON, THERE IS NO NEED TO PLACE A 1 IN FRONT OF THE NAME. • IF THERE ARE SUBSTITUENTS PRES ...
Παρουσίαση του PowerPoint
Παρουσίαση του PowerPoint

... Before and during these syntheses, groups of chemists sitting around blackboards or piles of paper plan the work they are about to undertake. Possible routes are drawn out, criticized, modified again when the behavior of the compounds in the flask turns out to be different from what was expected, un ...
Document
Document

Bimolecular reactions of the chromium
Bimolecular reactions of the chromium

... insertion into C-H and C-C bonds. Besides the investigation of the reactivity of bare metal ions, a study of the modification of the reactivity of the central metal ions of mrdinatively unsaturated metal complexes by the ligands is a major field of research in metal-organic chemistry.2 Usually the c ...
ALDEHYDES AND KETONES
ALDEHYDES AND KETONES

... C O H Methanal (formaldehyde) ...
Enhanced diastereoselectivity of an ene hydroperoxidation reaction
Enhanced diastereoselectivity of an ene hydroperoxidation reaction

... performing singlet oxygen ene reactions, with significant enhancement of product regioselectivity.1 It is found that, in the intrazeolite photooxygenation of geminal dimethyl trisubstituted alkenes, formation of the new double bond in the ene adducts occurs preferentially at the methyl groups.2 Labe ...
Boiling-Point Elevation of a Solution
Boiling-Point Elevation of a Solution

... Aldehydes and ketones share the carbonyl functional group which features carbon doubly bonded to oxygen. In the case of ketones there are two carbon atoms bonded to the carbonyl carbon and no hydrogens. In the case of aldehydes there is at least one hydrogen bonded to the carbonyl carbon, the other ...
Organic Chemistry-II
Organic Chemistry-II

67 Preview of Carbonyl Chemistry Kinds of carbonyls 1. Aldehydes
67 Preview of Carbonyl Chemistry Kinds of carbonyls 1. Aldehydes

... products (C-C bond forming reaction) Formation of Gilman reagents, R can be alkyl, vinyl or aryl but not alkynyl. ...
part 1
part 1

CaCl2.2H2O assisted oxidation of alcohols with (NH4)2Cr2O7
CaCl2.2H2O assisted oxidation of alcohols with (NH4)2Cr2O7

... dichromate in the presence of CaCl2.2H2O (Table I, Scheme I). The reaction is simply performed by stirring a mixture of alcohol, (NH4)2Cr2O7 and CaCl2.2H2O in an oil-bath (60°C) for the appropriate time (Table I). Alcohols were oxidized efficiently and the corresponding carbonyl compounds were isola ...
102 Lecture Ch15
102 Lecture Ch15

Chapter 20 Amines-part 2
Chapter 20 Amines-part 2

... (H 3PO2) to replace the diazonium group with a hydrogen atom t This reaction can be used to remove an amino group that was ...
Asymmetric (stereoselective) synthesis
Asymmetric (stereoselective) synthesis

Chapter 17 Aldehydes and Ketones
Chapter 17 Aldehydes and Ketones

... The functional group of an aldehyde is a carbonyl group bonded to a hydrogen atom. • In methanal, the simplest aldehyde (formaldehyde), the carbonyl group is bonded to two hydrogens. • In other aldehydes, it is bonded to one hydrogen and one carbon group. The functional group of a ketone is a carbon ...
Phosphine-Catalyzed Additions of Nucleophiles and Electrophiles to
Phosphine-Catalyzed Additions of Nucleophiles and Electrophiles to

... (8.7), HNEt3+ (10.7) in H2O), and therefore better leaving groups, they have strikingly different nucleophilic profiles. Tertiary phosphines are much stronger nucleophiles than corresponding amines. For example, the rate of the SN2 substitution of C2H5I with Et2PhP is more than 500 times faster than ...
EXPERIMENT 3: The Grignard Reaction: Synthesis of
EXPERIMENT 3: The Grignard Reaction: Synthesis of

... The reactions involved in the synthesis of complex organic molecules can commonly be categorized into either functional group interconversions or skeleton building reactions. The latter category, primarily those involving carbon-carbon bond formations, is most important in anabolic organic synthesis ...
Review Chapter 19
Review Chapter 19

... Oxidation of Alcohols to Carbonyl Compounds The oxidation of alcohols to carbonyl compounds is the reverse of nucleophilic addition (below). Most oxidants accept the alcohol oxygen as a nucleophile followed by loss of the acidic hydrogen. The process is completed by an E2-like elimination of h ...
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1,3-Dipolar cycloaddition

The 1,3-dipolar cycloaddition is a chemical reaction between a 1,3-dipole and a dipolarophile to form a five-membered ring. The earliest 1,3-dipolar cycloadditions were described in the late 19th century to the early 20th century, following the discovery of 1,3-dipoles. Mechanistic investigation and synthetic application were established in the 1960s, primarily through the work of Rolf Huisgen. Hence, the reaction is sometimes referred to as the Huisgen cycloaddition (this term is often used to specifically describe the 1,3-dipolar cycloaddition between an organic azide and an alkyne to generate 1,2,3-triazole). Currently, 1,3-dipolar cycloaddition is an important route to the regio- and stereoselective synthesis of five-membered heterocycles and their ring-opened acyclic derivatives.
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