798555-68-7

Upstream product

• 798555-60-9 2-[acetoxy(5-phenylisoxazol-3-yl)methyl]acrylic acid methyl ester 
• 640292-08-6 2-[hydroxy-(5-phenylisoxazol-3-yl)methyl]acrylic acid methyl ester 
• 831181-22-7 2-(5-phenylisoxazol-3-ylmethyl)acrylic acid methyl ester 

Downstream Products

• 798555-63-2 4-amino-2-methyl-6-oxo-6-phenyl-hex-4-enoic acid methyl ester 
• 831181-42-1 (Z)-3-methyl-5-(2-oxo-2-phenylethylidene)pyrrolidin-2-one 

Relevant academic research and scientific papers

Simple and efficient synthesis of substituted 2-pyrrolidinones, 2-pyrrolones, and pyrrolidines from enaminones of Baylis-Hillman derivatives of 3-isoxazolecarbaldehydes

(Chemical Equation Presented). The enaminones, generated from derivatives of appropriately substituted Baylis-Hillman adducts of 3-isoxazolecarbaldehydes, undergo intramolecular ring-closure reactions to afford substituted 2-pyrrolidinones, 1,5-dihydro-2-

Studies on the catalytic hydrogenation of Baylis-Hillman derivatives of substituted isoxazolecarbaldehydes. Unusual retention of isoxazole ring during Pd-C-promoted hydrogenation of Baylis-Hillman adducts

Results of the catalytic hydrogenation of Baylis-Hillman adducts obtained from substituted 3-, 4- and 5-isoxazolecarbox-aldehydes and their corresponding acetates in the presence of Raney-Ni and Pd-C are presented. The hydrogenation of Baylis-Hillman addu