Archives for Chemistry Experiments of 2-(4-Bromobutoxy)tetrahydro-2H-pyran

If you are interested in 31608-22-7, you can contact me at any time and look forward to more communication.Related Products of 31608-22-7

Related Products of 31608-22-7, Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.31608-22-7, Name is 2-(4-Bromobutoxy)tetrahydro-2H-pyran, molecular formula is C9H17BrO2. In a patent, introducing its new discovery.

Coupling reactions of lithium compounds, (Z)-carbonyl olefination of phosphonium ylides and ‘crossed’ Wittig olefination of bisylides are the key reaction steps in the synthesis principle for nonconjugated, bisolefinic Lepidoptera pheromones and structural analogs. Double unsaturated (E,Z)- and (E,E)-1-vinyl halides are converted into the corresponding (E,Z)- and (E,E)-1-vinyl lithium compounds and coupled selectively to (E,Z)- and (E,E)-alkadienols, alkadienals and alkadienyl acetates with different carbon chain length, geometry and relative positions of double bonds. ‘Crossed’ Wittig reactions of 1,omega-alkylidene bisylides with two different alkanals gives rise to the formation of corresponding (Z,Z)-dienic sex attractants and derivatives. A monounsaturated (E)-1-vinyl iodide is the synthon for the preparation of an (E)-alkenyl bromide which is converted to an (E)-alkenyl phosphonium salt and (Z)-selectively olefinated to (Z,E)-isomers of moth sex pheromones.

If you are interested in 31608-22-7, you can contact me at any time and look forward to more communication.Related Products of 31608-22-7

Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics