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Synlett 1993; 1993(9): 699-700
DOI: 10.1055/s-1993-22577
DOI: 10.1055/s-1993-22577
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Synthesis of Two Novel Spiro Lactones Related to the B/C Ring System of Bakkenolides by Radical Cyclization
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Publikationsverlauf
Publikationsdatum:
19. März 2002 (online)
The preparation of spiro lactones 2a and 2b was achieved by photochemically induced free-radical cyclization of allyl 1-(phenylseleno)-3-methyl-2-oxo-3-cyclopentenecarboxylate (4a) and its 4-methyl isomer (4b), respectively, followed by selenoxide elimination.