109754-25-8Relevant academic research and scientific papers
Reactions of aliphatic diazo compounds: VI. Reactions of diazomethane and ethyl diazoacetate with (E)-2-arylmethylene-1,2,3,4-tetrahydronaphthalen-1-ones
Molchanov,Korotkov,Kostikov
, p. 470 - 473 (2004)
Diazomethane and ethyl diazoacetate add to (E)-2-arylmethylene-1,2,3,4- tetrahydronaphthalen-1-ones in a regio- and stereoselective fashion, yielding the corresponding 4'-aryl-1,2,3,4,4',5'-hexahydro-3'H-naphthalene-2-spiro-3'- pyrazol-1-ones. The products formed by addition of ethyl diazoacetate undergo isomerization into 4,5-dihydro-1H-pyrazole derivatives.
Synthesis and Stereochemistry of Spiropyrazolines
Toth, Gabor,Szoelloesy, Aron,Levai, Albert,Kotovych, George
, p. 1895 - 1898 (2007/10/02)
Spiropyrazolines have been synthesized by 1,3-dipolar cycloaddition of an 2-arylidene-1-tetralone, 3-arylidene-chromanones, -1-thiochromanones, and -flavanones with diazomethane.The relative configuration and stereochemistry of the products have been dete
