59159-53-4Relevant academic research and scientific papers
A highly efficient and stereoselective cycloaddition of nitrones to N-arylitaconimides
Teterina, Polina S.,Efremova, Mariia M.,Sirotkina, Ekaterina V.,Novikov, Alexander S.,Khoroshilova, Olesya V.,Molchanov, Alexander P.
supporting information, (2019/08/26)
The 1,3-dipolar cycloaddition of keto- and aldonitrones with N-arylitaconimides proceeds regioselectively giving only 5-spiroisoxazolidines. In the case of aldonitrones the reaction proceeds with high diastereoselectivity. A range of the obtained adducts
Highly efficient and stereoselective cycloaddition of nitrones to indolyl- and pyrrolylacrylates
Dmitriev, Viktor A.,Efremova, Mariia M.,Novikov, Alexander S.,Zarubaev, Vladimir V.,Slita, Alexander V.,Galochkina, Anastasia V.,Starova, Galina L.,Ivanov, Andrey V.,Molchanov, Alexander P.
supporting information, p. 2327 - 2331 (2018/05/25)
The reactions of various nitrones with indolyl- and pyrrolylacrylates proceeds regioselectively with high diastereoselectivity in the case of aldonitrones, and represents an effective method for obtaining new indolyl- and pyrrolyl-substituted isoxazolidin
Regio- and stereoselectivity of cycloaddition of C-amidonitrones to esters of methylenecyclopropanedicarboxylic acids
Molchanov,Tung, Tran Q.,Kostikov
experimental part, p. 269 - 276 (2011/05/04)
C-Amidonitrones add regio- and stereoselectively to esters of 3-methylenecyclopropane-1,2-dicarboxylic, 2-(diphenylmethylene)cyclopropane-1,1- dicarboxylic, and 2-(1-phenylethylidene)cyclopropane-1,1-dicarboxylic acids to form a single diastereomer of 4-spirocyclopropaneisoxazolidines.
