107402-99-3Relevant academic research and scientific papers
Cycloaddition of Nitrones with Allenes. An Example of Steric Control of Regiochemistry
Padwa, Albert,Kline, Donald N.,Koehler, Konrad F.,Matzinger, Michael,Venkatramanan, M. K.
, p. 3909 - 3917 (2007/10/02)
A study of the cycloaddition behavior of a series of electron-deficient allenes with C-phenyl-N-alkylnitrones has been carried out.The 1,3-dipolar cycloaddition proceeds in high yield with complete regiospecifity toproduce 5-methylene substituted isoxazol
ISOXAZOLINE OXIDATION. AN EFFICIENT METHOD FOR THE PREPARATION OF α,β-UNSATURATED CARBONYL COMPOUNDS
Padwa, Albert,Kline, Donald N.,Perumattam, John
, p. 913 - 916 (2007/10/02)
MCPBA peracid oxidation of Δ4-isoxazolines derived from the dipolar cycloaddition reaction of nitrones with acetylenes or allenes produces α,β-unsaturated ketones in excellent yield.
DIPOLAR CYCLOADDITION REACTION OF (PHENYLSULFONYL)PROPADIENE WITH NITRONES AND ALKYLATION STUDIES OF THE CYCLOADDUCTS
Padwa, Albert,Carter, Stephen P.,Chiacchio, Ugo,Kline, Donald N.
, p. 2683 - 2686 (2007/10/02)
Dipolar cycloaddition of nitrones with (phenylsulfonyl)propadiene give 4-sulfonyl substituted isoxazolidenes whose reactions with base and several electrophiles have been studied.
