6708-14-1Relevant articles and documents
Synthesis of Spiro[2.2]pentanes and Spiro[2.3]hexanes Employing the Me3Al/CH2I2 Reagent
Ramazanov, Ilfir R.,Kadikova, Rita N.,Zosim, Tat'yana P.,Dzhemilev, Usein M.,de Meijere, Armin
, p. 7060 - 7067 (2017/12/28)
Substituted alkylidenecyclopropanes reacted with 5 equivalents each of Me3Al and CH2I2 at room temperature in hexane to give 1-mono- and 1,1-disubstituted spiro[2.2]pentanes in high yields. Surprisingly, the same reaction
Ring strain release as a strategy to enable the singlet state photodecarbonylation of crystalline 1,4-cyclobutanediones
Kuzmanich, Gregory,Garcia-Garibay, Miguel A.
experimental part, p. 883 - 888 (2012/01/13)
Challenging most chemists' intuition, highly reactive dialkyl biradicals can be reliably generated in the solid state by taking advantage of the photodecarbonylation of cyclic ketones. However, it has been shown that radical stabilizing groups with resonance-delocalizing abilities at the α-carbons of the precursor are required to facilitate the α-cleavage reaction, and that triplet state reactivity is essential to slow down the combination of the intermediate acyl-alkyl biradical back to the starting ketone. Relatively long triplet acyl-alkyl biradical lifetimes give a chance for the loss of CO to occur. Looking for additional strategies to generate transient biradicals in solids, we studied the solid state photochemistry of four aliphatic, dispiro-substituted 1,4-cyclobutandiones (1a-d) that were expected to react from the singlet state. We hypothesized that the release of ring strain from the small ring carbonyl would make the reverse acyl-alkyl combination disfavored, allowing for the loss of CO to occur efficiently and irreversibly. We report here the results of studies carried out in solution, bulk (powder) crystals, and nanocrystalline photochemistry. We have recently shown that excitation of dispirocyclohexyl-1,3-cyclobutanedione 1c led to the trapping of the intermediate oxyallyl with a half life of about 42 min. Our studies with the three other crystalline derivatives revealed that, while all react efficiently, the remarkably long lifetime of oxyallyl is unique to crystals of 1c.
Synthesis of energetic compounds via the metathesis reaction of 4-methylenespiro[2,3]hexane
Kotov,Chernykh,Finkel'shtein,Strel'chik,Tyshchenko,Milovantseva
experimental part, p. 309 - 313 (2010/03/24)
Transformations of methylenespiro[2,3]hexane (MSH) on a heterogeneous rhenium-alumina metathesis (disproportionation) catalyst were studied. It was found that, owing to a significant difference in the stability of carbenic complexes of methylene and disubstituted carbenes, MSH undergoes isomerization to 4-methylspiro[2,3]hex-4-ene followed by their cometathesis yielding bis(spiro[2,3]hexylidene-4). The feasibility of selective cometathesis of MSH and dicyclobutylidene on the rhenium-alumina catalyst resulting in the formation of 4-cyclobutylidenespiro[2,3]hexane was shown.
Preparative-Scale Syntheses of Bicyclobutylidene, Methylenecyclobutane and Cyclobutanone
Fitjer, Lutz,Quabeck, Ulrike
, p. 299 - 300 (2007/10/02)
One-pot syntheses of bicyclobutylidene (3) and methylenecyclobutane (4) are described.Both 3 and 4 are valuable precursors of cyclobutanone (5).
