Search results
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
- | group10 = [[Aldehyde]]s4 KB (317 words) - 16:53, 27 September 2010
- | group1 = [[Aldehyde]]s7 KB (590 words) - 21:04, 24 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