2007
Susana Rojas-Lima, Lidia Santillan-Sid, Heraclio López-Ruiz, y Alejandro Alvarez-Hernandez. Diastereoselective synthesis of spiro-beta-lactams via staudinger reaction. Heterocycles 71, 531-542 (2007). DOI: 10.3987/COM-06-10942
Abstract
In this work, eleven new spiro-?-lactams have been prepared using the Staudinger reaction of isomaleimides (1a-d) and carboxylic acids (chloroacetic acid, (-)-menthoxyacetic acid (7) and an oxazolidinone derived acid (10)) in the presence of triphosgene under mild condition. All reactions have been shown to be stereoselective. The new stereogenic centers were assigned by X-ray diffraction.
Furocoumarins of three species of the genus Dorstenia
Bis(acetylsalicylato-j2O,O00)diaquacadmium(II)
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio
Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes
Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.