Search Results - "Caple, R."

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    Stepwise Electrophilic Addition. Some Novel Synthetic Ramifications of an Old Concept by Smit, William A, Caple, Ron, Smoliakova, Irina P

    Published in Chemical reviews (01-12-1994)
    “…The strategy of modern organic synthesis is focused on the incorporation of convergency points into protocols designed for the preparation of complex…”
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    Polyfunctional Compounds Containing the 4,6-Dialkoxy-7-arylthioheptene Moiety as Synthetically Useful Intermediates. The Course of Lewis Acid-Induced Transformations by Chekmarev, Dmitriy S, Lazareva, Margarita I, Zatonsky, Georgy V, Maskaev, Andrei V, Caple, Ron, Smit, William

    Published in Journal of organic chemistry (15-11-2002)
    “…Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products…”
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    Reaction of vinyl ethers with ArSCl adducts of d-glucal by Smoliakova, Irina P., Han, Mingming, Gong, Jianchun, Caple, Ron, Smit, William A.

    Published in Tetrahedron (09-04-1999)
    “…Lewis acid mediated reactions of vinyl ethers with ArSCl adducts of benzyl protected D-glucal followed by quenching of the five-membered sulfonium salt…”
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    New Synthesis of Tetrahydro-L,4-Thiazine-3-Ones from 1,2-Aminopropanethiols and α-Chlorocarboxylic Acids by Magerramov, A. M., Allakhverdiev, A. M., Akhmedova, Z. I., Caple, R., Zhdankin, V. V.

    Published in Synthetic communications (01-02-1999)
    “…Tetrahydro-l,4-thiazine-3-ones 5 can be efficiently prepared by the condensation of 1,2-aminopropanethiols 1 and sodium chlorocarboxylates 4 under basic…”
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    Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety by Chekmarev, Dmitrii S., Maskaev, Andrei V., Zatonsky, Georgy V., Lazareva, Margarita I., Caple, Ron, Smit, William A.

    Published in Mendeleev communications (2001)
    “…The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the…”
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