Studies Toward the Synthesis of Lomaiviticins and Englerins

 

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Part I: Lomaiviticins A and B are novel C2-symmetric dimeric molecules with profound cytotoxic activity. The most challenging feature of these molecules is the densely functionalized central core. We envisioned the synthesis of the lomaiviticin core by an unprecedented Diels-Alder dimerization of ortho- quinols and masked ortho-benzoquinones, followed by the fragmentation of the extra carbon-carbon bond. This chapter describes the stereoselective elaboration of the ortho-quinol and masked ortho- benzoquinone dimers to the fragmentation precursors and the unsuccessful attempts to effect the scission of the extra bond. Part II: Englerin A is a new guaiane sesquiterpene and has been shown to be a selective renal cancer inhibitor. We envisioned the synthesis of englerin A via a novel strategy featuring Wagner-Meerwein rearrangement followed by intramolecular cation trapping. This chapter describes the stereoselective synthesis of the key cis-decalin intermediate from (-)-carvone and the unsuccessful attempts to realize the skeletal rearrangement.

Product Specifications
SKU :COC98359
AuthorSrinivas Achanta
LanguageEnglish
BindingPaperback
Number of Pages116
Publishing Year2011-07-15T00:00:00.000
ISBN978-3639369885
Edition1 st
Book TypeOrganic chemistry
Country of ManufactureIndia
Product BrandNot defined
Product Packaging InfoBox
In The Box1 Piece
Product First Available On ClickOnCare.com2015-08-18 00:00:00
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