32595-98-5Relevant articles and documents
Synthesis of xyloketal A, B, C, D, and G analogues
Pettigrew, Jeremy D.,Wilson, Peter D.
, p. 1620 - 1625 (2007/10/03)
A series of demethyl analogues of the natural products xyloketal A, B, C, D, and G have been prepared in a notably direct manner from 3-hydroxymethyl-2- methyl-4,5-dihydrofuran and a series of corresponding phenols. These syntheses featured a boron trifluoride diethyl etherate-promoted electrophilic aromatic substitution reaction as a key step. In the case of the synthesis of analogues of xyloketal A, the process was found to be highly efficient (up to 93% yield). The optimized isolated yield of these reaction products is remarkable in view of the fact that this transformation involves, minimally, six individual reactions. Moreover, these synthetic studies provide significant insight into the possible biogenic origin of the xyloketal natural products.
Heteroannulation of 4-oxo-4H-1-benzopyrans (chromosomes) via the conjugate addition of haloalkanols in the presence of base
Cremins,Hayes,Wallace
, p. 9431 - 9438 (2007/10/02)
Chromones (4-oxo-4H-1-benzopyrans) bearing electron-withdrawing substituents at C-3 react with 2-haloethanols and potassium carbonate in acetone to produce tetrahydrofuro[2,3-b][1]benzopyran-4-ones, the heteroannulation proceeding via the conjugate addition of the haloethanol to the chromone, followed by intramolecular alkylation. Under the conditions of the reaction, the products derived from chromone-3-carbaldehydes undergo in situ deformylation.
Dye-Sensitized Photooxygenation of 2,3-Dihydrofurans: Competing Cycloadditions and Ene Reactions of Singlet Oxygen with a Rigid Cyclic Enol Ether System
Gollnick, Klaus,Knutzen-Mies, Karen
, p. 4017 - 4027 (2007/10/02)
Singlet oxygen reacts with 2,3-dihydrofuran (1), 5-methyl (7), 4,5-dimethyl- (13), and 4-carbomethoxy-5-methyl-2,3-dihydrofuran (20), 5,6-dimethyl-3,4-dihydro-2H-pyran (26), and 3-methoxy-2-methyl-2-butene (32) in nonpolar and polar aprotic solvents to yield dioxetanes and allylic hydroperoxides, except 32, which gives only allylic hydroperoxides.The dioxetanes were isolated, but decompose slowly with weak chemiluminescence at room temperature to yield the corresponding dicarbonyl compounds.The allylic hydroperoxides produced by the cyclic enol ethers could not be isolated or separated by high vacuum distillation or by chromatography; the endocyclic allylic hydroperoxides arising from the dihydrofurans eliminate H2O2 to yield the corresponding furans while the exocyclic allylic hydroperoxides gives unknown products.Allylic hydroperoxides 28 and 29 and the dioxetane 27 obtained from 26 yield the same dicarbonyl compound 31.The proportion of dioxetanes to allylic hydroperoxides depends on ring size and substitution of the enol ethers and on solvent polarity.Smaller ring size, greater electron-donor substitution, and solvent polarity favor the formation of dioxetanes at the expense of allylic hydroperoxides.It is noteworthy that enol ether 20, an α,β-unsaturated ester, forms appreciable amounts of a dioxetane in polar solvents (44 percent in acetonitrile).Kinetic results show that the rate and product distribution of the ene reaction are independent of solvent polarity, whereas the rate of dioxetane formation increases with solvent polarity.It is suggested that cycloadditions and ene reactions occur via different transition states and intermediates, zwitterions and perepoxides, respectively.Furthermore, the remarkable propensity to dioxetane formation of dihydrofurans compared to that of dihydropyrans and the other enol ethers seems to be due to the rigidity of the five-membered ring in the transition state and intermediate zwitterion.
