OpenAlex 268 works 2 author topics
Works
268 works
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 95.9%
A novel class of chiral 5,5'-di(2,4,6-trialkyl)aryl salen-metal complexes have been developed and shown to catalyze highly enantioselective Nazarov cyclization reactions, giving rise to cyclopentenoids in 90:10-98:2 er. Significantly, the catalysts also promote, for the first time, highly enantioselective Nazarov reac…
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YÖKSİS
SJR Q1
JCR Q2
OpenAlex top 10%
OpenAlex 96.7%
No abstract yet.
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YÖKSİS
SJR Q3
JCR Q3
OpenAlex top 10%
OpenAlex 91.6%
Organocatalysis is an emerging and new field towards the direction of asymmetric synthesis and has shown a tremendous growth in 21st century. As the demand for chiral pharmaceuticals and chiral organic molecules is increasing immensely, different types of organocatalysts have been developed and used from time to time.…
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SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 94.3%
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSymmetry-Driven Synthesis of Indole Alkaloids: Asymmetric Total Syntheses of (+)-Yohimbine, (-)-Yohimbone, (-)-Yohimbane, and (+)-AlloyohimbaneJeffrey Aube, Shomir Ghosh, and Mehmet TanolCite this: J. Am. Chem. Soc. 1994, 116, 20, 9009–9018Publication Date (Print):October 1,…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 95.4%
A problem has arisen in using chiral shift reagents (CSR) and chiral solvating agents (CSA) to determine meso and racemic forms of diastereoisomers in which the stereogenic centers of the molecules are separated by achiral spacers. It is found that NMR signals of both meso and racemic forms of diastereoisomers may exh…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 95.4%
A problem has arisen in using chiral shift reagents (CSR) and chiral solvating agents (CSA) to determine meso and racemic forms of diastereoisomers in which the stereogenic centers of the molecules are separated by achiral spacers. It is found that NMR signals of both meso and racemic forms of diastereoisomers may exh…
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Exceptionally high turnover frequencies recorded for a new chitosan-based palladium(II) catalyst 2016YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.8%
No abstract yet.
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Exceptionally high turnover frequencies recorded for a new chitosan based palladium II catalyst 2016YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.8%
No abstract yet.
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Exceptionally high turnover frequencies recorded for a new chitosan based palladium II catalyst 2016YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.8%
No abstract yet.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 92.5%
No abstract yet.
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OpenAlex 88.9%
No abstract yet.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex 81.0%
Various chiral (9-anthryl)carbinol templates undergo Diels-Alder cycloadditions with a variety of symmetric and nonsymmetric dienophiles with excellent pi-facial selectivity and regioselectivity, under both thermal and Lewis acid catalyzed conditions.
Academicians
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