1,824,213 research outputs found

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014jp

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014DO

    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014

    No full text
    C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014C-271 ENTREGA IPN PREMIO DE ENSAYO INNOVACIÓN EDUCATIVA 2014PD

    An Efficient Synthesis of the Taxane-Derived Anticancer Agent ABT-271

    No full text
    ABT-271, 1, has been identified as a promising anticancer agent. ABT-271 is a novel taxane possessing a C9-(R)-hydroxyl group as opposed to a C9-ketone which is present in Taxol and Taxotere. To further evaluate ABT-271 as a potential anticancer agent, an efficient synthesis was developed which allows the large scale synthesis of ABT-271. Ketalization of the 7,9-diol of 9-DHAB-III, 2, allows selective removal of the C13-acetate with phenyllithium. The resulting C13-hydroxyl group is then acylated using LiHMDS and β-lactam 22 to give ABT-271 in protected form. The protecting groups were removed first by acidic hydrolysis followed by basic hydrolysis to provide ABT-271. Application of this synthetic sequence provided over 600 g of ABT-271, 1
    corecore