Umwandlung in Enol - ορισμός. Τι είναι το Umwandlung in Enol
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Τι (ποιος) είναι Umwandlung in Enol - ορισμός

CHEMICAL COMPOUND
Acedicon; Dihydrocodeine enol acetate; Acetyldihydrocodeinone; Dihydrocodeinone enol acetate; ATC code R05DA10; ATCvet code QR05DA10

Stereochemistry of ketonization of enols and enolates         
  • Keto-enediol equilibrium for [[ribulose-1,5-bisphosphate]].
  • doi=10.1021/ja00203a019}}</ref>
  • '''Keto-enediol tautomerizations.''' Enediol in the center; [[acyloin]] isomers at left and right. Ex. is [[hydroxyacetone]], shown at right.
  • 220px
CHEMICAL COMPOUND HAVING A HYDROXYL GROUP ATTACHED TO A CARBON ATOM CONNECTED TO ANOTHER CARBON ATOM VIA DOUBLE BOND
Keto–enol tautomerism; Enolate ion; Keto-enol tautomer; Enolization; Alkenol; Erlenmeyer rule; Keto enol tautomery; Keto-enol tautomerization; Enediol; Enol-keto tautomerism; Stereochemistry of ketonization of enols and enolates; User:Hezimmerman/sub page; User:Hezimmerman/User:Hezimmerman/Stereochemistry of Ketonization of Enols and Enolates; Kinetic Protonation; User:Hezimmerman/Stereochemistry of Ketonization of Enols and Enolates; Kinetic Protonation; Stereochemistry of Ketonization of Enols and Enolates; Kinetic Protonation; Ketonization of enols; Enols; Keto-enol tautomerism
In the stereochemistry of ketonization of enols and enolates, theory is provided explaining the diastereoselectivity(a)"Overlap Control of Carbanionoid Reactions. I.
Phenylpyruvate tautomerase         
CLASS OF ENZYMES
EC 5.3.2.1; Phenylpyruvate keto---enol-isomerase
In enzymology, phenylpyruvate tautomerase or Macrophage migration inhibitory factor () is an enzyme that catalyzes the chemical reaction
Enol ether         
  • [[Enamine]]s are chemically related to enol ethers.
  • 352px
  • [[Ethyl vinyl ether]] is a potent [[anesthetic]].
CLASS OF CHEMICAL COMPOUNDS
Vinyl ethers
In organic chemistry an enol ether is an alkene with an alkoxy substituent. The general structure is R2C=CR-OR where R = H, alkyl or aryl.

Βικιπαίδεια

Thebacon

Thebacon (INN; pronounced ), or dihydrocodeinone enol acetate, is a semisynthetic opioid that is similar to hydrocodone and is most commonly synthesised from thebaine. Thebacon was invented in Germany in 1924, four years after the first synthesis of hydrocodone. Thebacon is a derivative of acetyldihydrocodeine, where only the 6–7 double bond is saturated. Thebacon is marketed as its hydrochloride salt under the trade name Acedicon, and as its bitartrate under Diacodin and other trade names. The hydrochloride salt has a free base conversion ratio of 0.846. Other salts used in research and other settings include thebacon's phosphate, hydrobromide, citrate, hydroiodide, and sulfate.