Search results

...09}}</ref><ref name=eros>{{cite book |doi=10.1002/047084289X.ra026|chapter=Acetyl Cyanide|title=Encyclopedia of Reagents for Organic Synthesis|year=2001|last Acetyl cyanide is also prepared by [[hydrocyanation]] of [[ketene]]: ...

...plit under acidic conditions into [[hexanol]] and the [[zwitterion]]ic [[3-acetyl-1-(3-sulfopropyl)pyridinium]]. [[MALDI matrix]] compounds such as [[alpha-Cyano-4-hydroxycinnamic acid|α-cyano-4-hydroxycinnamic acid ...

:Acetyl-CoA + Butyrate <math>\rightleftharpoons</math> Acetate + Butyryl-CoA :Acetyl-CoA + Succinate <math>\rightleftharpoons</math> Acetate + Succinyl-CoA ...

| Name = CO-methylating acetyl-CoA synthase | caption = Monomeric Acetyl-CoA synthase ...

==Related compounds== [[Acetyl nitrate]] is a nitrate anhydride, being derived from the condensation of ni ...

{{short description|Chemical reaction involving repeated halogenation of an acetyl group (–COCH3)}} ...ic Press, New York, '''1978'''</ref> The reaction can be used to transform acetyl groups into [[carboxyl group]]s ({{chem2|R\sC(\dO)OH}}) or to produce [[chl ...

...the synthesis of [[Alcohol (chemistry)|alcohol]]s and other [[bio-based]] compounds. A significant limitation for further engineering with this strain is the l ...CoA pathway uses only 4.<ref>{{Cite web |date=2017-05-09 |title=5.12G: The Acetyl-CoA Pathway |url=https://bio.libretexts.org/Bookshelves/Microbiology/Microb ...

...antane came to be known, was only the second member of an entire family of compounds known as the diamondoids. The synthesis of the third member of the series i ...anes of up to 35 carbons and coke, as well. The assumption that diamondoid compounds can be synthesized through thermal cracking requires more verification.<ref ...

...the final step of the pathway. Thus the main interest in these [[chemical compounds]] has been in the study of [[chlorophyll]] biosynthesis in [[plants]], [[al ...ides and Roseobacter denitrificans, and a Common Hydratase Mechanism for 3-acetyl Group Formation |year=1996 |last1=Porra |first1=Robert J. |last2=Schafer |f ...

...he binding of acetylcholine to the anionic site of the cholinesterase, the acetyl group of acetylcholine can bind to the esteratic site. Important amino acid ...the acetylcholine to the esteratic site of the cholinesterase. Because the acetyl group can't bind the cholinesterase, the acetylcholine can't be cleaved. Th ...

...= McKervey|first2 = M. A.|title = Organic Synthesis with α-Diazo Carbonyl Compounds|journal = [[Chem. Rev.]]|year = 1994|volume = 94|issue = 4|pages = 1091–116 ...10.1002/anie.197500321|title = The Wolff Rearrangement of α-Diazo Carbonyl Compounds}}</ref><ref>{{cite journal|year = 2002|journal = [[Eur. J. Org. Chem.]]|aut ...

...ember of the [[group 10 element|group 10]] of the [[periodic table]]. Most compounds in the group have an [[oxidation state]] of +2. Nickel is classified as a [ ...s, as nickel is adjacent to copper and iron in the periodic table can form compounds with the same structure as the [[high-temperature superconductor]]s that ar ...

{{Short description|Group of chemical compounds}} ...58 |pmid=11909873|doi-access=free }}</ref> an ''N''-acyl terminus (usually acetyl),<ref name="Wiest-2002" /> and high levels of ''α'',''α''-dialkylated non-p ...

...ous group of [[prokaryote]]s which can degrade and utilize [[hydrocarbon]] compounds as source of carbon and energy. Despite being present in most of environmen ...diazophilic, i.e. they can live in environments extremely poor in nitrogen compounds, which allows them to distribute themselves throughout the environment. The ...

...el butyrate, nickel caprylate, nickel lactate, nickel benzoate, nickel bis(acetyl acetonate), nickel salicylate, nickel alkyl phenyl salicylate. Nickel stear [[Nickel succinate]] can form [[metal organic framework]] compounds.<ref>{{cite journal |last1=Guillou |first1=Nathalie |last2=Livage |first2=C ...

...example of a [[Schotten-Baumann reaction]]. [[Benzylamine]] reacts with [[acetyl chloride]] under Schotten-Baumann conditions to form ''N''-benzylacetamide. ...-permeable to {{chem|H|2}}, but not to {{CO2}}, effectively separating the compounds.<ref name=":0" /><ref name=":4" /> ...

| metabolites = [[Acetaldehyde]]; [[Acetic acid]]; [[Acetyl-CoA]]; [[Carbon dioxide]]; [[Ethyl glucuronide]]; [[Ethyl sulfate]]; [[Prop ...ily member 2 [[ACSS2]] (EC 6.2.1.1) and acetyl-CoA synthase 2 ([[ACSS1]]). acetyl-CoA then participates in the [[citric acid cycle]].<ref name="AcademicPress ...

...00121a010|pmid=1737021|citeseerx=10.1.1.539.2952}}</ref> or identify small compounds,<ref>{{Cite journal|last1=Caligiani|first1=A.|last2=Acquotti|first2=D.|last ...=10.1016/0016-7037(80)90155-6|bibcode=1980GeCoA..44..649S}}</ref> as these compounds are easily separated. Another advantage of methane for compound-specific me ...