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Organophosphorus compounds synthesis

Bu sayfa OpenAlex konu etiketine göre çalışmaları ve o konuda görünen akademisyenleri listeler. YÖKSİS temel alan / yan dal değildir.

OpenAlex 717 eser 23 yazar konusu

Çalışmalar

717 eser

  1. Chiral configurations in cyclophosphazene chemistry 2015
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 97.0%

    Özet henüz yok.

  2. Chiral configurations in cyclophosphazene chemistry 2015
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 97.0%

    Özet henüz yok.

  3. Phosphorus–nitrogen compounds part 27. Syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of new phosphazenes bearing secondary amino and pendant (4-fluorobenzyl)spiro groups 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.7%

    Özet henüz yok.

  4. Phosphorus nitrogen compounds part 27 Syntheses structural characterizations antimicrobial and cytotoxic activities and DNA interactions of new phosphazenes bearing secondary amino and pendant 4 fluorobenzyl spiro groups 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.7%

    Özet henüz yok.

  5. Phosphorus nitrogen compounds part 27 Syntheses structural characterizations antimicrobial and cytotoxic activities and DNA interactions of new phosphazenes bearing secondary amino and pendant 4 fluorobenzyl spiro groups 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.5%

    Özet henüz yok.

  6. Phosphorus-nitrogen compounds part 27. Syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of new phosphazenes bearing secondary amino and pendant (4-fluorobenzyl)spiro groups 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.5%

    Özet henüz yok.

  7. Phosphorus nitrogen compounds part 27 Syntheses structural characterizations antimicrobial and cytotoxic activities and DNA interactions of new phosphazenes bearing secondary amino and pendant 4 fluorobenzyl spiro groups 2013
    YÖKSİS OpenAlex 85.5%

    Özet henüz yok.

  8. Generation of Acyl Anion Equivalents from Acylphosphonates via Phosphonate Phosphate Rearrangement A Highly Practical Method for Cross Benzoin Reaction 2005
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 83.8%

    [reactions: see text] Acylphosphonates are potent acyl anion precursors that generate acyl anion equivalents under the promotion of cyanide anion via phosphonate-phosphate rearrangement. These anions readily react with aldehydes to provide cross-benzoin products. In this way it is possible to synthesize a variety of a…

  9. Phosphorus Nitrogen Compounds 21 Syntheses Structural Investigations Biological Activities and DNA Interactions of New N O Spirocyclic Phosphazene Derivatives The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents 2010
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 92.5%

    The reactions of hexachlorocyclotriphosphazatriene, N(3)P(3)Cl(6), with N/O-donor-type N-alkyl (or aryl)-o-hydroxybenzylamines (1a-1e) produce mono- (2a-2e), di- (3a-3d), and tri- (4a and 4b) spirocyclic phosphazenes. The tetrapyrrolidino monospirocyclic phosphazenes (2f-2i) are prepared from the reactions of partly s…

  10. Phosphorus−Nitrogen Compounds. 21. Syntheses, Structural Investigations, Biological Activities, and DNA Interactions of New N/O Spirocyclic Phosphazene Derivatives. The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents 2010
    OpenAlex üst %10 OpenAlex 92.4%

    The reactions of hexachlorocyclotriphosphazatriene, N(3)P(3)Cl(6), with N/O-donor-type N-alkyl (or aryl)-o-hydroxybenzylamines (1a-1e) produce mono- (2a-2e), di- (3a-3d), and tri- (4a and 4b) spirocyclic phosphazenes. The tetrapyrrolidino monospirocyclic phosphazenes (2f-2i) are prepared from the reactions of partly s…

  11. Phosphorus Nitrogen Compounds 21 Syntheses Structural Investigations Biological Activities and DNA Interactions of New N O Spirocyclic Phosphazene Derivatives The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents 2010
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 92.4%

    The reactions of hexachlorocyclotriphosphazatriene, N(3)P(3)Cl(6), with N/O-donor-type N-alkyl (or aryl)-o-hydroxybenzylamines (1a-1e) produce mono- (2a-2e), di- (3a-3d), and tri- (4a and 4b) spirocyclic phosphazenes. The tetrapyrrolidino monospirocyclic phosphazenes (2f-2i) are prepared from the reactions of partly s…

  12. Phosphorus Nitrogen Compounds 21 Syntheses Structural Investigations Biological Activities and DNA Interactions of New N O Spirocyclic Phosphazene Derivatives The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents 2010
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 92.4%

    The reactions of hexachlorocyclotriphosphazatriene, N(3)P(3)Cl(6), with N/O-donor-type N-alkyl (or aryl)-o-hydroxybenzylamines (1a-1e) produce mono- (2a-2e), di- (3a-3d), and tri- (4a and 4b) spirocyclic phosphazenes. The tetrapyrrolidino monospirocyclic phosphazenes (2f-2i) are prepared from the reactions of partly s…

Akademisyenler

23 akademisyen