Synthesis of cyclopropanes via organoiron methodology: preparation of the C9–C16 alkenylcyclopropane segment of ambruticin

Authors

Julie Lukesh, Marquette UniversityFollow
William Donaldson, Marquette UniversityFollow

Document Type

Article

Publication Date

2005

Publisher

Royal Society of Chemistry

Source Publication

Chemical Communications

Source ISSN

1359-7345

Abstract

A synthesis of the C9–C16 segment of ambruticin is described which relies on organoiron methodology to establish the 1,2,3-trisubstituted cyclopropane ring.

Comments

Accepted version. Chemical Communications, Issue 1 (2005) pp 110-112. DOI: 10.1039/B413129K. © 2005 Royal Society of Chemistry. Used with permission.

Recommended Citation

Lukesh, Julie and Donaldson, William, "Synthesis of cyclopropanes via organoiron methodology: preparation of the C9–C16 alkenylcyclopropane segment of ambruticin" (2005). Chemistry Faculty Research and Publications. 55.
https://epublications.marquette.edu/chem_fac/55