In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Application In Synthesis of 3-Iodotetrahydrofuran, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 121138-01-0, name is 3-Iodotetrahydrofuran. In an article£¬Which mentioned a new discovery about 121138-01-0
(-3-ketotetrahydrofuran-2-yl) ethanal derivatives and a method for their preparation
Compounds having utility in medicine in countering cellular malfunction e.g. in conditions embraced by the general term “cancer”, which compounds normally exist us a keto-enol tautomeric pair, the racetalc keto form of which is rapresented by formula (Ia), wherein R is a hydrogen, lower alkyl, acyl, or another functional group of up to 6 carbons including at least one hetero atom, which atom may be directly bonded to the beta-carbon, which compound may be in the acylic form shown or in a cyclic form as equilibrium keto-enol tautomer derivatives and anomeric forms thereof, including enantiomers when R is hydrogen and diastereoisomers when R is another group. A method of obtaining such a compound comprises selecting an appropriate dihydrofuran having a protected primary alcohol side chain in the 2-position, subjecting the said protected alcohol side chain-substituted dihydrofuran to oxidation using a chromium-based reagent to yield the corresponding acid, subjecting said acid to iodolaetonisation conditions to yield the cis,cis,trans-trisubstituted iodo-lactone which upon displacement of the iodine provides the cis,cis,cis-tri-substituted hydroxylacetone which is capable of being reduced to obtain a lactol which is in equilibrium with the corresponding open chain aldehyde. STR1
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 121138-01-0, help many people in the next few years.Application In Synthesis of 3-Iodotetrahydrofuran
Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem