Srikrishna, Adusumilli and Nagaraju, Sankuratri and Venkateswarlu, Somepalli and Hiremath, Uma S and Reddy, Jagadeeswar T and Venugopalan, Paloth (1999) A formal total synthesis of (±)-homogynolide-B. In: Journal Of The Chemical Society-Perkin Transactions 1 (15). pp. 2069-2076.
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A formal total synthesis of (+/-)-homogynolide-B, a sesquiterpene containing an alpha-spiro-beta-methylene-gamma-butyrolactone moiety spirofused to a bicyclo[4.3.0]nonane framework, is described. Thus, Hagemann's ester 11 was converted into the allyl alcohol 16 in three steps. One-pot Claisen rearrangement of the allyl alcohol 16 and 2-methoxypropene in the presence of a catalytic amount of propionic acid afforded a 3:2 epimeric mixture of the ketone 15 and further rearranged product 19. Ozonolysis followed by intramolecular aldol condensation and hydrogenation transformed the enones 15a,b into the key intermediate keto ketals 13a and 13b. Methoxymethylene Wittig reaction followed by bromoacetalisation converted the keto ketal 13a into the radical precursor bromo acetal 22a. The 5-exo-dig radical cyclisation of the bromo acetal 22a, followed by acid catalysed hydrolysis and oxidation, led to the keto spirolactone 12, Greene's precursor of homogynolide-B. The same sequence transformed the keto ketal 13b into a 3:2 mixture of the spirolactones 12 and 25, which on equilibration furnished the spirolactone 12. The stereostructure of the keto spirolactone 12 was unambiguously established by single-crystal X-ray diffraction analysis.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Royal Society of Chemistry.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||22 Jul 2009 07:52|
|Last Modified:||19 Sep 2010 04:58|
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