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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/17245
Title: β-Fragmentation of alkoxy radicals. An approach to the synthesis of ring a of vernolepin
Authors: Francisco, Cosme G.; Freire, Raimundo; Rodríguez Morales, María S.; Suárez, Ernesto
Issue Date: 1987
Publisher: Elsevier
Citation: Tetrahedron Letters 28(29): 3397-3400 (1987)
Abstract: A model of ring A of vernolepin is synthesized by 1,4-fragmentation of γ-thiyl and γ-stannyl alkoxy-radicals, generated by photolysis of the corresponding δ-lactols (4) and (5) in the presence of iodosobenzene diacetate and iodine. It should be pointed out that the δ-lactone ring and the angular vinyl group are introduced in one step.
Description: 4 pages, 1 table, 2 schemes.
Publisher version (URL): http://dx.doi.org/10.1016/S0040-4039(00)95523-0
URI: http://hdl.handle.net/10261/17245
ISSN: 0040-4039
DOI: 10.1016/S0040-4039(00)95523-0
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