2003
DOI: 10.1002/anie.200352094
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A Modular Approach to Oxoindolizino Quinolines: Efficient Synthesis of Mappicine Ketone (Nothapodytine B)

Abstract: A general route to oxoindolizino quinolines, such as nothapodytine A, mappicine, camptothecin, and several chemotherapeutic derivatives, is illustrated by the synthesis of the antiviral natural product from Nothapodytes foetida, mappicine ketone (R1=R4=H, R2=CH3, R3=COC2H5). A wide range of new camptothecinoids should now be readily available for biological testing.

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Cited by 33 publications
(8 citation statements)
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“…Our group demonstrated the versatility of the method through the synthesis of the angiotensin converting enzyme inhibitor (À)-A58365A (52), (AE)-ipalbidine (53), b-carbolinone 54 and a variety of other novel indolizidine-based compounds. 20 The use of 50 as a key intermediate in total synthesis has also been demonstrated by Greene and coworkers 21 in a recent synthesis of the antiviral agent mappicine ketone, one of the alkaloids isolated together with campothecin from the Indian plant Nothapodytes foetida.…”
Section: Alkaloid Synthesis Using Isomu¨nchnones As Key Intermediatesmentioning
confidence: 88%
“…Our group demonstrated the versatility of the method through the synthesis of the angiotensin converting enzyme inhibitor (À)-A58365A (52), (AE)-ipalbidine (53), b-carbolinone 54 and a variety of other novel indolizidine-based compounds. 20 The use of 50 as a key intermediate in total synthesis has also been demonstrated by Greene and coworkers 21 in a recent synthesis of the antiviral agent mappicine ketone, one of the alkaloids isolated together with campothecin from the Indian plant Nothapodytes foetida.…”
Section: Alkaloid Synthesis Using Isomu¨nchnones As Key Intermediatesmentioning
confidence: 88%
“…71 The synthesis of 144 began with formation of the known cycloadduct 139a (R 1 = H; R 2 = CO 2 Me) by cycloaddition of the isomünchnone dipole derived from diazo sulfone 138 with methyl acrylate (Scheme 27). [67][68][69][70] This multistep sequence proceeded smoothly and in high yield when catalyzed by rhodium(II) acetate.…”
Section: Mappicine Ketonementioning
confidence: 99%
“…They show a diversity of bioactive properties such as antitumor, antimicrobial, anti-inflammatory, cardiotonic, antiviral, and antimalarial activity . These scaffolds are also important intermediates in many organic transformations . A series of methods have been developed for the synthesis of 1,6-annulated 2-pyridones and 2,3-annulated 4-pyrimidinones such as intramolecular nucleophilic substitution, radical cyclization, intramolecular alkenylation, and intramolecular Heck reaction.…”
mentioning
confidence: 99%