4893-00-9

Upstream product

• 5006-22-4 Cyclobutanecarbonyl chloride 
• 96999-02-9 α-bromocyclopropanecarboxylic acid chloride 
• 70339-23-0 1-bromo-1-cyclobutanecarboxylic acid chloride 
• 6708-14-1 1,1'-bi(cyclobutylidene) 
• 40052-11-7 2-bromo-3-methyl-but-2-enoyl chloride 

Downstream Products

• 4415-97-8 dicyclobutyl ketone 
• 6708-14-1 1,1'-bi(cyclobutylidene) 
• 59078-45-4 cyclobutylidenemethanone 
• 1207374-91-1 13-phenyl-12-oxadispiro[3.1.3.3]dodecane-5,11-dione 

Relevant academic research and scientific papers

Ring strain release as a strategy to enable the singlet state photodecarbonylation of crystalline 1,4-cyclobutanediones

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.

A new rotane family: Synthesis, structure, conformation, and dynamics of [3.4]-, [4.4]-, [5.4]-, and [6.4]rotane

The synthesis, structure, conformation, and dynamics of a new rotane family consisting of four-membered rings are described. All syntheses are based on bicyclobutylidene (9): [2+1] cycloaddition of cyclobutylidene yields [3.4]rotane (5) (9-5), [2+2] cyclo

LOW TEMPERATURE KETENE PREPARATIONS USING NITROSYLTETRACARBONYLCHROMIUM (-II) ANION

Methylene and cyclopropyl ketenes can be generated at -100 deg C by the dehalogenation of α-bromoacylhalides using nitrosyltetracarbonylchromium (-II) anion.This facilitates the trapping of these ketenes with more stable ketenes to give mixed ketene dimers.