160946-53-2Relevant academic research and scientific papers
Enantioselective syntheses and resolution of the key White intermediate for the synthesis of trisporic acids
Bacigaluppo, Jose A.,Colombo, Maria I.,Preite, Marcelo D.,Zinczuk, Juan,Ruveda, Edmundo A.,Sieler, Joachim
, p. 1041 - 1057 (1996)
Two asymmetric syntheses of the alkylated cyclohexenone carboxylic acid moiety, the key White intermediate (4a), of trisporic acids A, B and C are described. The syntheses feature a Michael addition in tandem with an aldol condensation as the central step
Enantioselective Synthesis of the White Key Intermediate for the Synthesis of Trisporic Acids
Bacigaluppo, Jose A.,Colombo, Maria I.,Cravero, Raquel M.,Gonzalez-Sierra, Manuel,Preite, Marcelo D.,et al.
, p. 1877 - 1880 (1994)
The asymmetric construction of the alkylated cyclohexenone carboxylic acid moiety of trisporic acids A, B and C and the syntheses of related precursors are described.The syntheses feature a Michael addition in tandem with an aldol condensation as the cent
