「Aldehydes」の共起表現(1語右で並び替え)

「Aldehydes」の共起表現一覧(1語右で並び替え)

Aldehydes

1語右で並び替え

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Organic reduction of aldehydes, alkenes, alkynes, nitro compounds, oxiranes
s the photochemical cleavage or homolysis of aldehydes and ketones into two free radical intermedia
y or secondary alcohols to the corresponding aldehydes and ketones.
These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols
iles, for deprotecting acetals and ketals to aldehydes and ketones, and for converting epoxides int
hesis: they will oxidize primary alcohols to aldehydes and then to carboxylic acids, and secondary
orted a method for synthesis of alkenes from aldehydes and ketones using compounds called phosphoni
It is used to purify or isolate aldehydes and ketones.
Human skin also contains aldehydes and gets stained as well.
Aldehydes and ketones do not react with it.
f sulfoxides, reductive coupling of aromatic aldehydes and reduction of aldehydes
Sodium sulfite forms a bisulfite adduct with aldehydes, and with ketones forms a sulfonic acid.
llyl-, allenyl-, or propargylstannanes to an aldehydes and imines)
s dehydration of acyclic primary alcohols to aldehydes and ketones.
rmate can be used for reductive amination of aldehydes and ketones (Leuckart reaction)
ates in the same kinds of reactions as other aldehydes and other aromatic compounds.
Aldehydes and formic acid (and formic acid esters) als
an efficiently reduce aliphatic and aromatic aldehydes, and it is less active on hexoses.
yed as a catalyst for the cyanosilylation of aldehydes and ketones.
ely test for carbonyl groups associated with aldehydes and ketones.
hydrogen gas, and reduces carboxylic esters, aldehydes, and ketones to alcohols.
the corresponding alkyl fluorides as well as aldehydes and unhindered ketones to geminal difluoride
s and ketones can be prepared by reaction of aldehydes and esters with Ruppert's reagent.
dithiol is mainly used for the protection of aldehydes and ketones via their reversible formation o
zing aliphatic nitro compounds to less-toxic aldehydes and ketones.
ynthesis can be used to produce a variety of aldehydes and became known as the Darzens reaction and
es, cinnamaldehyde, condensation products of aldehydes and amines (imines), chromates, phosphates,
de (oxidization) to create hypohalous acids, aldehydes and carboxylic acids.. Ozone is not as commo
Phenolic aldehydes are a type of natural phenol.
Typically, in organic synthesis, ketones and aldehydes are protected as their dioxolanes instead of
Phenolics aldehydes can be found in wines and cognacs.
n - The conversion of alcohols to ketones or aldehydes can be effected by metal catalysts such as c
ns, linear and branched paraffins, alcohols, aldehydes, carboxylic acids, and aromatic compounds.
ns, linear and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic compounds.
ns, linear and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic compounds.
e used in organic chemistry to form names of aldehydes containing the -(CO)H group.
it readily forms oximes with keto acids and aldehydes, especially the pyridoxal phosphate cofactor
ionalities (such as esters, ketones, amides, aldehydes, etc.).
o play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid pe
s react similarly (adding two R groups), but aldehydes give by-products.
He experimented and manipulated the aldehydes in Quelque Fleurs, resulting in a fragrance
ic heterocycle oxazole from cyanohydrins and aldehydes in the presence of anhydrous hydrochloric ac
ember catalyzes the reduction of a number of aldehydes, including the aldehyde form of glucose, and
chenko reaction (catalytic transformation of aldehydes into esters).
f the dithiolanes and dithianes derived from aldehydes is that the methyne group can be deprotonate
The reaction of the Schiff reagent with aldehydes is complex with several research groups repo
oamines and diamines, ethanolamines, amides, aldehydes, ketones and chlorinated aromatics.
ct with a wide range of carbonyls, including aldehydes, ketones and esters.
the presence of water to carbonyl compounds: aldehydes, ketones, peroxides.
rom the sun oxidize unburned hydrocarbons to aldehydes, ketones, and dicarbonyl compounds, whose se
s carbonyl derivatives including unsaturated aldehydes, ketones, and esters.
ong chain aliphatic hydrocarbon alcohols and aldehydes like octanol and octanal are second importan
for an amine group on the carbonyl carbon of aldehydes or ketones when reacted with ammonia or a pr
hoxide to form indene-oxalic ester, and with aldehydes or ketones in the presence of alkali to form
Under each of these conditions, aromatic aldehydes react much faster, but less stereoselectivel
primary enzyme responsible for oxidising the aldehydes that are produced by the 2-keto acid oxidore
(CNBr) activation and reductive amination of aldehydes to attach proteins to the agarose resin thro
reatly increases the ratio of straight-chain aldehydes to branched-chain aldehydes in the product m
talyze chemoselective addition of cyanide to aldehydes to give the cyanohydrins.
(OCH3)4 has been used to convert ketones and aldehydes to the corresponding ketals and acetals, res
tituted alkenes based on the condensation of aldehydes with metallated 1-phenyl-1H-tetrazol-5-yl su
etals can be obtained by reacting ketones or aldehydes with thioles.
The condensation of aldehydes with hydroxylamine gives aldoxime, and ketox