Showing 1 - 20 results of 32 for search '"Mitsunobu reaction"', query time: 0.15s Refine Results
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    Synthetic studies of sumalactones A - D and Raistrickindole A by Pham, Thang Loi

    Published 2023
    “…The N- hydroxyDKP can be synthesised asymmetrically by an intramolecular Mitsunobu reaction of a chiral hydroxamic acid.…”
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    Thesis-Doctor of Philosophy
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    N-hydroxy-alpha-amino phosphonate derivatives as potential haptens for eliciting catalytic antibodies by Gouverneur, V, Lalloz, M

    Published 1996
    “…An efficient synthesis of N-hydroxy-α-amino phosphonate derivatives has been developed using a Mitsunobu reaction with N-phenoxycarbonyl-O-tert-butyl-alkoxycarbonyl hydroxylamine and α-hydroxy phosphonates.…”
    Journal article
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    Synthesis of excitatory amino acid analogues by Goundry, W, Lee, V, Baldwin, J

    Published 2006
    “…The key reactions involved were a Negishi coupling of Jackson's organozinc reagent with vinyl bromide 8 and subsequent ring closure of 15 and 16 using the Mitsunobu reaction. © Georg Thieme Verlag Stuttgart.…”
    Journal article
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    Convenient Preparation and Spectroscopic Characterization of 7<i>R</i>-Hydroxymatairesinol by Eleonora Colombo, Giuseppe Paladino, Umberto Ciriello, Daniele Passarella

    Published 2021-09-01
    “…The preparation of 7<i>R</i>-HMR (<i>allo</i>-hydroxymatairesinol) is reported by: (a) NaBH<sub>4</sub> kinetic reduction of 7<i>R</i>/7<i>S</i> diastereomeric mixture; and (b) epimerization of the C7 hydroxyl group by Mitsunobu reaction and subsequent ester hydrolysis. The availability of highly pure target compound (7<i>R</i>-HMR) made it possible to confirm the structure of the target compound and to complete the full spectroscopic characterization.…”
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    Article
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    Photomechanical effect in “side-chain” polyimides with low content of azopyridine chromophore by Jolanta Konieczkowska, Klaudia Nocoń-Szmajda, Agnieszka Ciemięga

    Published 2024-06-01
    “…The paper presents the photomechanical effect generated in new azo side-chain polyimides synthesized through a post-functionalization strategy involving the Mitsunobu reaction. Prepared azo polyimide foils were irradiated by a 405 nm diode-laser beam (intensity, I = 100 mW/cm2; polarization, Eǀǀx) for the generation of the photomechanical effect. …”
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    Article
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    Synthetic 2-Nitrocinnamates: Investigation of the Antifungal Action against Candida Species by Lázaro Gomes do Nascimento, Mayara Castro de Morais, José Klidenberg de Oliveira Júnior, Edeltrudes de Oliveira Lima, Damião Pergentino de Sousa

    Published 2023-01-01
    “…Therefore, in the present study, a series of fourteen alkyl and aryl derivatives from (E)-2-nitrocinnamic acid were obtained using Fischer esterification, nucleophilic substitution with halides, and Mitsunobu reaction. Esters were evaluated for antifungal activity against several strains of Candida spp. using nystatin as a positive control. …”
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    Article
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    Synthesis of (−)-Kopsifoline A and (+)-Kopsifoline E by Myeong, In-Soo, Avci, Nadide Hazal, Movassaghi, Mohammad

    Published 2022
    “…The vinylogous urethane substructure of this intermediate affords (-)-kopsifoline D via C3-C21 bond formation under the Mitsunobu reaction conditions, while it enables selective C17-functionalization en route to (-)-kopsifoline A and (+)-kopsifoline E.…”
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    Article
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