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  2. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    ch 3 (ch 2) 7 ch=ch(ch 2) 11 co 2 h + o 3 + 0.5 o 2 → ch 3 (ch 2) 7 co 2 h + ho 2 c(ch 2) 11 co 2 h A number of drugs and their intermediates have been produced by ozonolysis. [ 22 ] The use of ozone in the pharmaceutical industry is difficult to discern owing to confidentiality considerations.

  3. Methylpentene - Wikipedia

    en.wikipedia.org/wiki/Methylpentene

    Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]

  4. (2R)-2-Methylpent-4-enoic acid - Wikipedia

    en.wikipedia.org/wiki/(2R)-2-Methylpent-4-enoic_acid

    R)-2-Methylpent-4-enoic acid can be synthesized using a chiral auxiliary such an oxazolidinone derivative, popularized by David Evans. One route of synthesis consists of three steps: One route of synthesis consists of three steps:

  5. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    1-Pentene is an alpha-olefin.Most often, 1-pentene is made as a byproduct of catalytic or thermal cracking of petroleum or during the production of ethylene and propylene via thermal cracking of hydrocarbon fractions.

  6. File:Ozonolysis Scheme 2 examples.svg - Wikipedia

    en.wikipedia.org/wiki/File:Ozonolysis_Scheme_2...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses ...

  7. Lemieux–Johnson oxidation - Wikipedia

    en.wikipedia.org/wiki/Lemieux–Johnson_oxidation

    The Lemieux–Johnson reaction ceases at the aldehyde stage of oxidation and therefore produces the same results as ozonolysis. The classical Lemieux–Johnson oxidation often generates many side products, resulting in low reaction yields; however the addition of non-nucleophilic bases, such as 2,6-lutidine , can improve on this. [ 3 ]

  8. Griesbaum coozonolysis - Wikipedia

    en.wikipedia.org/wiki/Griesbaum_coozonolysis

    The oxime first reacts with the ozone to form the corresponding carbonyl oxide, undergoes 1,3-dipolar cycloaddition with the carbonyl reactant to form the cyclic ozonide, as usual for the Criegee intermediate in the ozonolysis of alkenes. If no carbonyl compound is used, the carbonyl oxide may dimerize and form 1,2,4,5-tetraoxanes.

  9. Perfluoro(2-methyl-3-pentanone) - Wikipedia

    en.wikipedia.org/wiki/Perfluoro(2-methyl-3...

    Perfluoro(2-methyl-3-pentanone) is a fluorinated ketone with the structural formula CF 3 CF 2 C(=O)CF(CF 3) 2, a fully-fluorinated analog of ethyl isopropyl ketone. It is used as an electronics coolant liquid and fire protection fluid sold commercially by 3M under brand names such as Novec 1230, Novec 649, and FK-5-1-12. It is also known as ...