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akaturk Akademik ölçüm

Akademisyen

CİHANGİR TANYELİ

PROFESÖR

ORTA DOĞU TEKNİK ÜNİVERSİTESİ FEN-EDEBİYAT FAKÜLTESİ KİMYA BÖLÜMÜ

Akademik özet YÖKSİS ve OpenAlex ayrı sayılır.
Makale 101
YÖKSİS101 OpenAlex0
Proje 66
Kitap 0
Bildiri 23

Atıf etkisi

OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 93
h-indeks 28 Türkiye yüzdelik dilimi: 99 Üniversitesinde h-indekse göre 26. / 997
i10-indeks
69
Toplam atıf
2.612
Türkiye’de üst %1,2
Makale başına
28,1
FWCI
1,62
1,00 = dünya ortalaması
Dünyada üst %1
0
Dünyada üst %10
18

h-indeks ve atıflar, bu akademisyenin YÖKSİS makalelerinden OpenAlex’te eşleşenlerin atıf sayılarından hesaplanır (Google Scholar, WoS veya Scopus değildir). Eşleşmeyen makalelerin atıfı dahil değildir.

Alan sıralaması

YÖKSİS ?

Dizin çeyrekleri

?
Scopus (SJR) 94
  • Q1 78
  • Q2 11
  • Q3 5
  • Q4 0
WoS (JCR) 94
  • Q1 35
  • Q2 51
  • Q3 8
  • Q4 0
TR Index TR Index

1 makale

OpenAlex atıf yüzdelik
  • Üst %1 0
  • Üst %10 18
  • Ort. 73.4%
  • n 95
Diğer sayımlar

Scopus (SJR)

  • YÖKSİS satırı 97

WoS (JCR)

  • YÖKSİS satırı 97

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Yayını olan dergiler

34 dergi
Scopus (SJR)
TR Index

Makale filtresi uygulandı. Dergi filtresi: Tetrahedron Asymmetry Filtreyi kaldır

Makale listesi

26 / 101 makale

  1. 2016 A bis Lewis basic 2 aminoDMAP prolinamide organocatalyst for application to the enantioselective synthesis of Warfarin and derivatives Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2016.04.001 YÖKSİS SJR Q2 JCR Q2 OpenAlex 82.1%
  2. 2012 A method for the synthesis of pyridine based C2 symmetrical chiral nucleophilic organocatalysts via Pd catalyzed coupling Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2012.11.007 YÖKSİS SJR Q1 JCR Q2 OpenAlex 67.5%
  3. 2012 Stereoselective synthesis of optically active cyclopenta c pyridines and tetrahydropyridines Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2012.04.016 YÖKSİS SJR Q1 JCR Q2 OpenAlex 57.5%
  4. 2011 Stereoselective synthesis of optically active dihydrofurans and dihydropyrans via a ring closing metathesis reaction Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2011.07.003 YÖKSİS SJR Q1 JCR Q2 OpenAlex 72.1%
  5. 2010 Stereoselective synthesis of optically active cyclopenta c pyrans and cyclopenta c furans by the intramolecular Pauson Khand reaction Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2010.02.016 YÖKSİS SJR Q1 JCR Q2 OpenAlex 67.1%
  6. 2008 Stereoselective synthesis of spirocyclic cyclopentapyrans by the Pauson Khand reaction on camphor tethered enynes Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2008.11.020 YÖKSİS SJR Q1 JCR Q2 OpenAlex 64.4%
  7. 2007 Asymmetric synthesis of novel 1 4 aminoalcohol ligands with norbornene and norbornane backbone use in the asymmetric diethylzinc addition to benzaldehyde Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2007.09.019 YÖKSİS SJR Q1 JCR Q1 OpenAlex 59.5%
  8. 2006 The first enzymatic resolution of quaternary acetoxy substituted cyclic ketones Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2006.04.012 YÖKSİS SJR Q1 JCR Q2 OpenAlex 50.2%
  9. 2006 Kinetic resolution of primary alcohols having remote stereogenic centers lipase mediated kinetic resolution of 3 chloro 3 arylpropanols Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2006.06.001 YÖKSİS SJR Q1 JCR Q2 OpenAlex 58.8%
  10. 2006 Conformational control on remote stereochemistry in the intramolecular Pauson Khand reactions of enynes tethered to homoallyl and homopropargyl alcohols Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2006.11.012 YÖKSİS SJR Q1 JCR Q2 OpenAlex 67.1%
  11. 2006 Chemoenzymatic synthesis of enantiomerically enriched 2 oxobicyclo m 1 0 alkan 3 yl acetate derivatives Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2006.01.004 YÖKSİS SJR Q1 JCR Q2 OpenAlex 66.7%
  12. 2006 Stereoselective synthesis of optically active cyclitol precursors via a chemoenzymatic method Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2006.11.002 YÖKSİS SJR Q1 JCR Q2 OpenAlex 5.4%
  13. 2005 The first enzymatic resolution of quaternary acetoxy unsaturated cyclohexenones and cyclopentenones Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2005.11.016 YÖKSİS SJR Q1 JCR Q2 OpenAlex 46.9%
  14. 2005 Asymmetric synthesis of 1 4 amino alcohol ligands with a norbornene backbone for use in the asymmetric diethylzinc addition to benzaldehyde Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2005.04.019 YÖKSİS SJR Q1 JCR Q2 OpenAlex 79.3%
  15. 2005 Enzymatic resolution of 2 endo hydroxymethyl and acetoxymethyl substituted hexachloronorbornene derivatives Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2005.06.014 YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.0%
  16. 2004 Enzyme catalyzed reverse enantiomeric separation of methyl 3 cyclohexene 1 carboxylate Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2004.05.034 YÖKSİS SJR Q1 JCR Q1 OpenAlex 45.5%
  17. 2004 Corrigendum to Resolution of anti 2 3 dioxabicyclo 2 2 2 oct 7 en 5 ol via Candida cylindracea lipase synthesis of and proto quercitol Tetrahedron Asymmetry 15 2004 453 Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2004.05.017 YÖKSİS SJR Q1 JCR Q1
  18. 2004 Chemoenzymatic synthesis of and acetoxylated cyclic ketones Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2004.04.019 YÖKSİS SJR Q1 JCR Q1 OpenAlex 69.6%
  19. 2004 Resolution of anti 2 3 dioxabicyclo 2 2 2 oct 7 en 5 ol via Candida cylindracea lipase synthesis of and proto quercitol Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2003.11.037 YÖKSİS SJR Q1 JCR Q1 OpenAlex 78.8%
  20. 2004 Enzymatic desymmetrization of meso 2 3 bis acetoxymethyl and bis hydroxymethyl substituted hexachloronorbornadiene derivatives Tetrahedron: Asymmetry DOI 10.1016/j.tetasy.2003.11.023 YÖKSİS SJR Q1 JCR Q1 OpenAlex 46.2%

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