Addition of the titanium enolates of 2-pyridylthioesters lo imines featuring easily removable chiral auxiliaries affords beta-lactams in a highly stereoselective fashion
STEREOSELECTIVE SYNTHESIS OF BETA-LACTAMS BY CONDENSATION OF TITANIUM ENOLATES OF 2-PYRIDYLTHIOESTERS WITH IMINES BEARING A CHIRAL AUXILIARY / R. ANNUNZIATA, M. BENAGLIA, M. CINQUINI, F. COZZI, L. RAIMONDI. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 34:43(1993), pp. 6921-6924.
STEREOSELECTIVE SYNTHESIS OF BETA-LACTAMS BY CONDENSATION OF TITANIUM ENOLATES OF 2-PYRIDYLTHIOESTERS WITH IMINES BEARING A CHIRAL AUXILIARY
R. ANNUNZIATAPrimo
;M. BENAGLIASecondo
;M. CINQUINI;F. COZZIPenultimo
;L. RAIMONDIUltimo
1993
Abstract
Addition of the titanium enolates of 2-pyridylthioesters lo imines featuring easily removable chiral auxiliaries affords beta-lactams in a highly stereoselective fashion
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