İçeriğe geç
akaturk Akademik ölçüm

OpenAlex konusu

Catalytic Alkyne Reactions

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

OpenAlex 216 eser 11 yazar konusu

Çalışmalar

216 eser

  1. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.9%

    Electrophilic cyclizations of α,β-alkynic hydrazones by molecular iodine were investigated for the synthesis of 4-iodopyrazoles. α,β-Alkynic hydrazones were readily prepared by the reactions of hydrazines with propargyl aldehydes and ketones. When treated with molecular iodine in the presence of sodium bicarbonate, α,…

  2. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.9%

    Electrophilic cyclizations of α,β-alkynic hydrazones by molecular iodine were investigated for the synthesis of 4-iodopyrazoles. α,β-Alkynic hydrazones were readily prepared by the reactions of hydrazines with propargyl aldehydes and ketones. When treated with molecular iodine in the presence of sodium bicarbonate, α,…

  3. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.9%

    Synthesis of pyrazoles via electrophilic cyclization of α,β-alkynic hydrazones by copper(I) iodide is described. When treated with copper(I) iodide in the presence of triethylamine in refluxing acetonitrile, α,β-alkynic hydrazones, prepared readily from hydrazines and propargyl aldehydes and ketones, undergo electroph…

  4. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.9%

    Synthesis of pyrazoles via electrophilic cyclization of α,β-alkynic hydrazones by copper(I) iodide is described. When treated with copper(I) iodide in the presence of triethylamine in refluxing acetonitrile, α,β-alkynic hydrazones, prepared readily from hydrazines and propargyl aldehydes and ketones, undergo electroph…

  5. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 97.6%

    The Sc(OTf)3-catalyzed (3 + 2)-annulation of donor-acceptor cyclopropanes and ynamides is described, providing the corresponding cyclopentene sulfonamides in good to excellent yield. Deprotection and hydrolysis of the resulting ensulfonamides delivers 2,3-substituted cyclopentanones with high diastereoselectivity.

  6. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 94.3%

    A concise and regioselective approach to the synthesis of chromenopyridine and chromenopyridinone derivatives was developed. The synthetic strategy relies on the O-propargylation of aromatic hydroxyaldehydes followed by reaction with propargylamine. The intramolecular cycloaddition reaction between the alkyne and azad…

  7. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.3%

    The chemistry of palladium complexes has no limits. Many domino processes (even multicomponent) are continuously appearing in the literature. Carbocyclic and heterocyclic molecules are efficiently prepared under the atom-economy principle using the smallest amount of the catalyst. The importance of the applications in…

  8. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.8%

    Supply chain: the polycyclic core of (-)-berkelic acid (1) was constructed in just one step from very simple starting materials. The total synthesis of 1 involves a seven-step linear sequence. Protection/deprotection steps were avoided and all but the last step were performed on a gram scale. This synthesis could solv…

  9. OpenAlex üst %10 OpenAlex 93.8%

    The tandem hydroamination-annulation reaction of 4-pentyne-nitriles in the presence of amine nucleophiles and a cooperatively operating catalyst system, consisting of Ph(3)PAuCl and Zn(ClO(4))(2), provides an efficient route to 2-aminopyrroles. Two regioisomeric 2-aminopyrroles were formed in moderate to good yields.

  10. YÖKSİS SJR Q1 JCR Q1 OpenAlex 86.4%

    Dihydrobenzisoxazoles are readily prepared in good yields by the [3 + 2] cycloaddition of oxaziridines and arynes. The reaction involves an unusual cleavage of the C-O bond of the oxaziridine and tolerates a variety of substituents on the oxaziridine and the o-(trimethylsilyl)aryl triflate to form aryl-, heteroaryl-,…

  11. YÖKSİS SJR Q1 JCR Q1 OpenAlex 88.5%

    Copper(I) and nickel(0) complexes catalyze the formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes, a reaction hitherto best catalyzed by silver salts. These catalysts based on earth abundant metals are not only competent, but the copper catalyst, in particular, promotes cycloadditions of pyrido[2…

  12. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.2%

    The gold-catalyzed reaction of pyrrole and indole oximes having a propargyl group attached to the nitrogen atom was studied. The selective 6-endo-dig mode of cyclization was observed for the terminal alkynes giving rise to the formation of pyrazine N-oxides in the presence of a gold catalyst. However, the reaction wit…

Akademisyenler

11 akademisyen