Addition of lithium acetylides and ethynyl magnesium bromide to chiral ortho substituted benzaldehyde tricarbonylchromium complexes 1 - 3 gives alkynyl alcohols 4 - 7 in good yields and with complete stereoselection. © 1993.

Baldoli, C., Delbuttero, P., Licandro, E., Maiorana, S., Papagni, A., Torchio, M. (1993). STEREOSELECTIVE ALKYNYLATION OF CHIRAL BENZALDEHYDE CHROMIUM TRICARBONYL COMPLEXES - SYNTHESIS OF OPTICALLY-ACTIVE ALKYNYL ALCOHOLS. TETRAHEDRON LETTERS, 34(49), 7943-7946 [10.1016/S0040-4039(00)61518-6].

STEREOSELECTIVE ALKYNYLATION OF CHIRAL BENZALDEHYDE CHROMIUM TRICARBONYL COMPLEXES - SYNTHESIS OF OPTICALLY-ACTIVE ALKYNYL ALCOHOLS

PAPAGNI, ANTONIO;
1993

Abstract

Addition of lithium acetylides and ethynyl magnesium bromide to chiral ortho substituted benzaldehyde tricarbonylchromium complexes 1 - 3 gives alkynyl alcohols 4 - 7 in good yields and with complete stereoselection. © 1993.
Articolo in rivista - Articolo scientifico
CHIRAL BENZALDEHYDE CHROMIUM TRICARBONYL COMPLEXES, STEREOSELECTIVE ALKYNYLATION
English
1993
34
49
7943
7946
none
Baldoli, C., Delbuttero, P., Licandro, E., Maiorana, S., Papagni, A., Torchio, M. (1993). STEREOSELECTIVE ALKYNYLATION OF CHIRAL BENZALDEHYDE CHROMIUM TRICARBONYL COMPLEXES - SYNTHESIS OF OPTICALLY-ACTIVE ALKYNYL ALCOHOLS. TETRAHEDRON LETTERS, 34(49), 7943-7946 [10.1016/S0040-4039(00)61518-6].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/32353
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