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From Self-sufficiency
- ...nd oxidation reactions. (9) is then converted to both a ketone (10) and an aldehyde (11).19 KB (2,731 words) - 17:52, 18 September 2010
- ...ilar to that produced by [[disulfiram]] (Antabuse), due to inhibition of [[aldehyde dehydrogenase]].<ref name=Goldfrank>{{cite book |author=Stork CM |editor=Ne4 KB (492 words) - 15:08, 6 July 2010
- ...roup, which arises from the reaction of the hydroxy group at C-5 and the [[aldehyde]] at C-1. Containing five carbon atoms and one oxygen atom, this ring is a23 KB (3,050 words) - 16:52, 27 September 2010
- ...α,β-epoxy [[ester]], which was [[decarboxylated]] and hydrolyzed to the aldehyde. Reaction with [[hydroxylamine]] gave the [[oxime]], converted to the [[nit29 KB (3,955 words) - 22:17, 21 September 2010
- ...he corresponding aldehyde/amine. The primary amine is then oxidized to an aldehyde followed by formation of the imine to yield the quinolizidine ring.<ref nam7 KB (891 words) - 09:44, 20 September 2010
- * Polyvinyl [[acetal]]s: Polyvinyl acetals are prepared by reacting [[aldehyde]]s with polyvinyl alcohol. [[Polyvinyl butyral]] (PVB) and polyvinyl formal7 KB (928 words) - 10:10, 20 September 2010
- ...r roasting temperature to Maillard products (reaction products between the aldehyde group of sugar and the alpha-amino-group of the amino acids). Further, [[di ...en coffee beans at 2 to 7 mg/1 kg); [[pentanal]] or [[valerianic aldehyde]] (very repulsive nauseating effect).<ref>{{cite book |author=Bessière-Tho29 KB (4,179 words) - 10:14, 20 September 2010
- ...e [[Open-chain compound|acyclic]] mono- and disaccharides contain either [[aldehyde]] groups or [[ketone]] groups. These [[carbonyl|carbon-oxygen]] double bond ...and hexoses can form [[ring structure]]s. In these closed-chain forms, the aldehyde or ketone group remains unfree, so many of the reactions typical of these g21 KB (2,875 words) - 10:14, 20 September 2010
- ...ther. A common example is [[glucose]] vs. [[fructose]]. The former is an [[aldehyde]], the latter is a [[ketone]]. Their interconversion requires either [[Gluc15 KB (2,242 words) - 10:17, 20 September 2010
- ...fatty acids, primary and [[secondary alcohol]]s, [[diol]]s, [[ketone]]s, [[aldehyde]]s.<ref name=Baker>EA Baker (1982) Chemistry and morphology of plant epicut11 KB (1,689 words) - 10:17, 20 September 2010
- ...line]], [[sodium nitrite]], [[cinnamaldehyde]], condensation products of [[aldehyde]]s and [[amine]]s ([[imine]]s), [[chromate]]s, [[nitrite]]s, [[phosphate]]s7 KB (1,003 words) - 10:17, 20 September 2010
- ''o''-Phenylenediamine condenses with [[ketone]]s and [[aldehyde]]s to give rise to a variety of useful products. Reactions with esters aff5 KB (609 words) - 13:10, 20 September 2010
- ...chsine stain for pancreatic islet beta cells<ref>Mowry RW, Emmel VM (1978) Aldehyde fuchsin staining, direct or after oxidation: problems and remedies, with sp3 KB (325 words) - 13:12, 20 September 2010
- | OtherNames = formol, methyl aldehyde, methylene oxide, methanal | Function = [[aldehyde]]s34 KB (4,726 words) - 21:35, 20 September 2010
- ...(at elevated temperatures), alkylating agents, [[carbon disulfide]], and [[aldehyde]]s and [[ketone]]s. Because of its bifunctional nature, having two amines,9 KB (1,089 words) - 20:14, 21 September 2010
- ...and Huber, R. | title = Crystal Structure of the Xanthine Oxidase-Related Aldehyde Oxido-Reductase from D-Gigas | journal = [[Science (journal)|Science]] | ye9 KB (1,258 words) - 20:15, 21 September 2010
- In this method, porphyrins are assembled from [[pyrrole]] and substituted [[aldehyde]]s. Acidic conditions are essential; formic acid, acetic acid, and propion12 KB (1,605 words) - 20:15, 21 September 2010
- This compound is widely used in organic chemistry because it reacts with [[aldehyde]]s and [[ketone]]s to give 1,3-[[dithiolane]]s, which are useful intermedia3 KB (410 words) - 20:15, 21 September 2010
- ...ines with natural bite angles near 120 °ree; increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation ...s believed that the ee isomer leads to the formation of more of the linear aldehyde, the desired product. In an effort to create rhodium complexes in which th12 KB (1,706 words) - 20:18, 21 September 2010
- ...diphenylphosphoryl azide]] in '''7''' and acid hydrolysis yields the azido aldehyde '''8'''. ...] of its anion (by reaction with [[Lithium diisopropylamide|LDA]] ) to the aldehyde group in '''8''' to form '''10''' as a mixture of [[epimer]]s. This is of n17 KB (2,355 words) - 22:15, 21 September 2010
- ...tion of activated [[aromatic rings]] such as [[phenols]], producing aryl [[aldehyde]]s in a reaction known as the [[Reimer-Tiemann reaction]]. Alternatively th21 KB (2,827 words) - 21:03, 24 September 2010