Enantioselective Synthesis of the Lomaiviticin Aglycon Full Carbon Skeleton Reveals Remarkable Remote Substituent Effects during the Dimerization Event
- 26 October 2010
- journal article
- research article
- Published by Wiley in Chemistry – A European Journal
- Vol. 16 (44) , 13058-13062
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Synthesis of the Fully Glycosylated Cyclohexenone Core of Lomaiviticin AOrganic Letters, 2009
- Synthesis of the Monomeric Unit of the Lomaiviticin AglyconAngewandte Chemie International Edition, 2009
- A Robust Platform for the Synthesis of New Tetracycline AntibioticsJournal of the American Chemical Society, 2008
- Total Synthesis of Kinamycins C, F, and JJournal of the American Chemical Society, 2007
- Total Synthesis of the Diazobenzofluorene Antibiotic (−)-Kinamycin CJournal of the American Chemical Society, 2006
- Studies on the Mechanism of Action of Prekinamycin, a Member of the Diazoparaquinone Family of Natural Products: Evidence for Both sp2 Radical and Orthoquinonemethide IntermediatesJournal of the American Chemical Society, 2006
- Stereocontrolled Synthesis of Model Core Systems of Lomaiviticins A and BAngewandte Chemie, 2006
- A Proposal for the Mechanism-of-Action of Diazoparaquinone Natural ProductsJournal of the American Chemical Society, 2005
- Lomaiviticins A and B, Potent Antitumor Antibiotics from Micromonospora lomaivitiensisJournal of the American Chemical Society, 2001
- An Efficient Synthesis of 3-Cyano-1(3H)-IsobehzofuranonesSynthetic Communications, 1987