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OpenAlex topic

Asymmetric Hydrogenation and Catalysis

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 1,135 works 49 author topics

Works

1,135 works

  1. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    Pentaphenylcyclopentadienyl ruthenium complexes (3) are excellent catalysts for the racemization of secondary alcohols at ambient temperature. The combination of this process with enzymatic resolution of the alcohols results in a highly efficient synthesis of enantiomerically pure acetates at room temperature with sho…

  2. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.5%

    Sodium borohydride, NaBH4, has been considered the most attractive hydrogen-storage material for portable fuel cell applications, as it provides a safe and practical means of producing hydrogen. In a recent communication (Zahmakiran, M.; Ozkar, S. Langmuir 2008, 24, 7065), we have reported a record total turnover numb…

  3. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.3%

    We describe a catalytic system composed of rhodium nanoparticles immobilized in a Lewis acidic ionic liquid. The combined system catalyzes the hydrogenation of quinolines, pyridines, benzofurans, and furan to access the corresponding heterocycles, important molecules present in fine chemicals, agrochemicals, and pharm…

  4. OpenAlex top 10% OpenAlex 97.7%

    Ferrocenyl-substituted aziridinylmethanol (Fam-1) was used as a catalyst with zinc for the asymmetric nitroaldol (Henry) reaction. This catalyst worked with a variety of aldehydes (aromatic, aliphatic, alpha,beta-unsaturated, and heteroaromatic) and alpha-ketoesters to give the nitroaldol product in up to 97% yield an…

  5. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.7%

    Ferrocenyl-substituted aziridinylmethanol (Fam-1) was used as a catalyst with zinc for the asymmetric nitroaldol (Henry) reaction. This catalyst worked with a variety of aldehydes (aromatic, aliphatic, alpha,beta-unsaturated, and heteroaromatic) and alpha-ketoesters to give the nitroaldol product in up to 97% yield an…

  6. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 96.9%

    Herein we report the discovery of a superior dimethylamine-borane dehydrogenation catalyst, more active than the prior best heterogeneous catalyst (Jaska, C. A.; Manners, I. J. Am. Chem. Soc. 2004, 126, 9776) reported to date for the dehydrogenation of dimethylamine-borane. The new catalyst system consists of rhodium(…

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

    A range of ruthenium cyclopentadienyl (Cp) complexes have been prepared and used for isomerization of allylic alcohols to the corresponding saturated carbonyl compounds. Complexes bearing CO ligands show higher activity than those with PPh3 ligands. The isomerization rate is highly affected by the substituents on the…

  8. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 96.7%

    A new type of carbene precursor, 1,5,6,7,8,8a-hexahydroimidazo[1,5- a ]pyridine ( 1 ), has been prepared from 2-(aminomethyl)piperidine and N,N -dimethylformamide dimethylacetal. The reactions of three imidazolidinium salts with [Rh(acac)(COD)] and [Ir(μ-OMe)(COD)] 2 were found to afford rhodium and iridium complexes…

  9. OpenAlex top 10% OpenAlex 98.7%

    The method for the synthesis of 1,4-dihydropyridine compounds in the presence of Pd–Ni–Ru@GO was developed, which is simple, effective and productive.

  10. YÖKSİS SJR Q2 JCR Q3 OpenAlex top 10% OpenAlex 98.7%

    The method for the synthesis of 1,4-dihydropyridine compounds in the presence of Pd–Ni–Ru@GO was developed, which is simple, effective and productive.

  11. YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.7%

    The method for the synthesis of 1,4-dihydropyridine compounds in the presence of Pd–Ni–Ru@GO was developed, which is simple, effective and productive.

  12. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 93.9%

    A highly effective and green procedure for the formation of α-alkylated ketones has been disclosed via the reaction of primary alcohols with secondary alcohols and ketones by using [IrCl(COD)(NHC)] complexes as a catalyst. Various α-alkylated ketones were obtained in high yields from the alkylation of alcohol with alc…

Academicians

49 academicians