ABSTRACT
The condensation of an enone or enal with cyanoacetamide derivatives and t-BuOK furnishes either 3-cyano-2-pyridones or 3-unsubstituted-2-pyridones, depending on whether the reaction is carried out in the presence or in the absence of O(2). In the first case, in situ oxidation of Michael-type intermediates takes place; in the second case, the products result from "decyanidative aromatization" of such intermediates. A one-step synthesis of 3-alkyl-2-pyridones has been devised on the basis of decyanative union of an enone/enal and a 2-alkylcyanoacetamide. The new reaction forms the centerpiece of an unusually concise synthesis of nothapodytine B (mappicine ketone).
Subject(s)
Chemistry, Organic/instrumentation , Chemistry, Organic/methods , Indolizines/chemical synthesis , Ketones/chemistry , Nitriles/chemistry , Pyridones/chemical synthesis , Quinolines/chemical synthesis , Alkanes/chemistry , Catalysis , Molecular Structure , Oxygen/chemistryABSTRACT
A synthetic method using tungsten-pi-allyl compounds is developed for total syntheses of natural bislactones including (+)-dihydrocanadensaolide (2), (+/-)-avenociolide (3), and (+/-)-isoavenociolide (4). Syntheses of these natural compounds are based on a common intermediate, trans-alpha-methylene butyrolactones bearing an anti-homoallylic alcohol. The kep steps in the syntheses involve an intramolecular alkoxycarbonylation of propargyltungsten complexes to yield tungsten-pi,gamma-lactonyl species, followed by condensation of their CpW(NO)I(pi-allyl) derivatives with suitable aldehydes. This new method is very efficient for the synthesis of (+/-)-avenociolide (3) and (+/-)-isoavenociolide (4). Total syntheses of compounds 3 and 4 require only six and three steps, respectively, on the basis of chloropropargyl derivatives.
