Synthesis of the C1–C16 fragment of ionomycin using a neutral (η<sup>3</sup>-allyl)iron complex
作者:John P. Cooksey、Philip J. Kocienski、Ying-fa Li、Stefan Schunk、Thomas N. Snaddon
DOI:10.1039/b606262h
日期:——
Key steps in the synthesis of the C1-C16 polyketide fragment of ionomycin were the nucleophilic addition of an organocuprate to a neutral (eta3-allyl)iron complex and the construction of a beta-diketone moiety by the Rh-catalysed rearrangement of an alpha-diazo-beta-hydroxyketone.