Enantioselective Synthesis of the C11-C24 Segment of Macrolactin a via Organoiron Methodology

Authors

Vadapalli Prahlad, Marquette UniversityFollow
William Donaldson, Marquette UniversityFollow

Document Type

Article

Language

eng

Publication Date

12-16-1996

Publisher

Elsevier

Source Publication

Tetrahedron Letters

Source ISSN

0040-4039

Abstract

The enantioselective synthesis of the Fe(CO)₃ completed C11-C24 segment of macrolactin A has been accomplished from rac-(methyl 6-oxo-2,4-hexadienoate)Fe(CO)₃ in 11 steps (>50% ee).

Comments

Tetrahedron Letters, Vol. 37, No. 51 (December 16, 1996): 9169-9172. DOI.

Recommended Citation

Prahlad, Vadapalli and Donaldson, William, "Enantioselective Synthesis of the C11-C24 Segment of Macrolactin a via Organoiron Methodology" (1996). Chemistry Faculty Research and Publications. 841.
https://epublications.marquette.edu/chem_fac/841