The use of a new and versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations of various chiral electrophiles is described. The method herein employed may represent an unprecedented and powerful tool for designing new synthetic strategies in the area of biologically relevant polyhydroxylated products

A New and Versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations / Caputo, Romualdo; Guaragna, Annalisa; Palumbo, Giovanni; Silvana, Pedatella. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 62:26(1997), pp. 9369-9371. [10.1021/jo9714627]

A New and Versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations

CAPUTO, ROMUALDO;GUARAGNA, ANNALISA;PALUMBO, GIOVANNI;
1997

Abstract

The use of a new and versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations of various chiral electrophiles is described. The method herein employed may represent an unprecedented and powerful tool for designing new synthetic strategies in the area of biologically relevant polyhydroxylated products
1997
A New and Versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations / Caputo, Romualdo; Guaragna, Annalisa; Palumbo, Giovanni; Silvana, Pedatella. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 62:26(1997), pp. 9369-9371. [10.1021/jo9714627]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/475919
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