2980-70-3Relevant academic research and scientific papers
Concerning Attempts To Synthesize out-Bicyclotetradec-1-ene Derivatives
Hamon, David P. G.,Krippner, Guy Y.
, p. 7109 - 7114 (1992)
The keto aldehydes 4-butanal (17), (E)-4-(6-oxocyclodec-1-enyl)butanal (24), and 4-(6-oxocyclodecylidene)butanal (7) have been synthesized.No bicyclotetradecadienes were found in the products from the zero-valent titanium reductive cyclization of compound 24.Instead, products arising from transannular reactions of the cyclodecyl ring system were isolated. 1,6-Divinylbicyclodecane (32) was obtained from the reductive cyclization of keto enal 7.The most plausible route for its formation is through a Cope rearrangement of a bicyclotetradecene derivative, suggesting that an out-bicyclotetradecenylbistitanium pinacolate 8 intervened.
Exceptionally high decarboxylation rate of a primary aliphatic acyloxy radical determined by radical product yield analysis and quantitative 1H-CIDNP spectroscopy
Fraind, Alicia,Turncliff, Ryan,Fox, Teri,Sodano, Justin,Ryzhkov, Lev R.
scheme or table, p. 809 - 820 (2012/06/29)
Symmetrical (RCO2CO2R; R=XCH2CH 2) and asymmetrical (RCO2CO2R′; R=C 9H19CH2CH2, R′=CH3 or m-ClC6H4) primary diacyl peroxides were thermally decomposed under different conditions to analyze the decarboxylation rates of the thermally generated acyloxy radicals. Quantitative models of the geminate product yields, and qualitative and quantitative 1H-CIDNP spectroscopy were used to obtain the decarboxylation rate estimates. Results reported here suggest that, unlike short chain acyloxy radicals such as propanoyloxyl, long chain acyloxy radicals possess the highest decarboxylation rates of all known acyloxy radicals, estimated at (0.5-1.5)× 10 12s-1 between 80 and 140°C. Given the nature of the dissociative state of acyloxy radicals, such rates appear to be the result of destabilization of the former by the steric bulk of the long chain substituents. Additionally, the rate of this order of magnitude suggests a nearly concerted decarboxylation of primary diacyl peroxides. Copyright
