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Beetalaktaamit (Finnish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Beetalaktaamit" in Finnish language version.

refsWebsite
Global rank Finnish rank
11doi.org
2nd place
10th place
9nih.gov
4th place
12th place
4harvard.edu
18th place
270th place
1ukim.edu.mk
low place
low place
1web.archive.org
1st place
1st place
1worldcat.org
5th place
9th place
1uva.nl
3,518th place
5,278th place
1dit.ie
low place
low place
1tcd.ie
5,099th place
low place

dit.ie

arrow.dit.ie

  • Niamh M. O. Boyle, Miriam Carr, Lisa M. Greene, Orla Bergin, Seema M. Mathwan, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents. Journal of Medicinal Chemistry, 16.11.2010. PubMed:21080725 doi:10.1021/jm101115u Artikkelin verkkoversio.

doi.org

dx.doi.org

  • Christian Brandt, Sascha D. Braun, Claudia Stein, Peter Slickers, Ralf Ehricht, Mathias W. Pletz, Oliwia Makarewicz: In silico serine β-lactamases analysis reveals a huge potential resistome in environmental and pathogenic species. Scientific Reports, 24.2.2017. PubMed:28233789 doi:10.1038/srep43232 Bibcode:2017NatSR...743232B
  • David E. Ehmann, Haris Jahić, Philip L. Ross, Rong-Fang Gu, Jun Hu, Gunther Kern, Grant K. Walkup, Stewart L. Fisher: Avibactam is a covalent, reversible, non–β-lactam β-lactamase inhibitor. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 2012, 109. vsk, nro 29, s. 11663–11668. PubMed:22753474 doi:10.1073/pnas.1205073109 Bibcode:2012PNAS..10911663E
  • D. J. Tipper, J. L. Strominger: Mechanism of action of penicillins: a proposal based on their structural similarity to acyl-D-alanyl-D-alanine. PNAS, 1965, 54. vsk, nro 4, s. 1133–1141. PubMed:5219821 doi:10.1073/pnas.54.4.1133 Bibcode:1965PNAS...54.1133T
  • Thomas T. Tidwell: Hugo (Ugo) Schiff, Schiff Bases, and a Century of β‐Lactam Synthesis. Angewandte Chemie, 25.1.2018, 47. vsk, nro 6, s. 1016–1020. PubMed:18022986 doi:10.1002/anie.200702965
  • Seyedmorteza Hosseyni, Aliasghar Jarrahpour: Recent advances in β-lactam synthesis. Organic & Biomolecular Chemistry, 2018, 16. vsk, nro 38, s. 6840–6852. PubMed:30209477 doi:10.1039/c8ob01833b
  • Nanda D. Paul, Andrei Chirila, Hongjian Lu, Peter Zhang, Bas de Bruin: Carbene Radicals in Cobalt(II)–Porphyrin‐Catalysed Carbene Carbonylation Reactions; A Catalytic Approach to Ketenes. Chemistry – a European Journal, 23.9.2013, 19. vsk, nro 38, s. 12953–12958. PubMed:24038393 doi:10.1002/chem.201301731
  • Andrei Chirila, Kaj M. van Vliet, Nanda D. Paul, Bas de Bruin: [Co(MeTAA)] Metalloradical Catalytic Route to Ketenes via Carbonylation of Carbene Radicals. European Journal of Inorganic Chemistry, 2018, nro 20–21. doi:10.1002/ejic.201800101 ISSN 1099-0682 Artikkelin verkkoversio.
  • Robert Burns Woodward: Penems and related substances. Philosophical Transactions of the Royal Society, 10.5.1980. PubMed:6109320 doi:10.1098/rstb.1980.0042 Bibcode:1980RSPTB.289..239W
  • Ashwini Nangia, Kumar Biradha, Gautam R. Desiraju: Correlation of biological activity in β-lactam antibiotics with Woodward and Cohen structural parameters—a Cambridge database study. Journal of the Chemical Society, Perkin Transactions 2, 1996, nro 5. doi:10.1039/p29960000943
  • Niamh M. O. Boyle, Miriam Carr, Lisa M. Greene, Orla Bergin, Seema M. Mathwan, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents. Journal of Medicinal Chemistry, 16.11.2010. PubMed:21080725 doi:10.1021/jm101115u Artikkelin verkkoversio.
  • Niamh M. O. Boyle, Lisa M. Greene, Orla Bergin, Jean-Baptiste Fichet, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis, evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones. Bioorganic & Medicinal Chemistry, 1.4.2011, 19. vsk, nro 7, s. 2306–2325. PubMed:21397510 doi:10.1016/j.bmc.2011.02.022 Artikkelin verkkoversio.

harvard.edu

adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Christian Brandt, Sascha D. Braun, Claudia Stein, Peter Slickers, Ralf Ehricht, Mathias W. Pletz, Oliwia Makarewicz: In silico serine β-lactamases analysis reveals a huge potential resistome in environmental and pathogenic species. Scientific Reports, 24.2.2017. PubMed:28233789 doi:10.1038/srep43232 Bibcode:2017NatSR...743232B
  • David E. Ehmann, Haris Jahić, Philip L. Ross, Rong-Fang Gu, Jun Hu, Gunther Kern, Grant K. Walkup, Stewart L. Fisher: Avibactam is a covalent, reversible, non–β-lactam β-lactamase inhibitor. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 2012, 109. vsk, nro 29, s. 11663–11668. PubMed:22753474 doi:10.1073/pnas.1205073109 Bibcode:2012PNAS..10911663E
  • D. J. Tipper, J. L. Strominger: Mechanism of action of penicillins: a proposal based on their structural similarity to acyl-D-alanyl-D-alanine. PNAS, 1965, 54. vsk, nro 4, s. 1133–1141. PubMed:5219821 doi:10.1073/pnas.54.4.1133 Bibcode:1965PNAS...54.1133T
  • Thomas T. Tidwell: Hugo (Ugo) Schiff, Schiff Bases, and a Century of β‐Lactam Synthesis. Angewandte Chemie, 25.1.2018, 47. vsk, nro 6, s. 1016–1020. PubMed:18022986 doi:10.1002/anie.200702965
  • Seyedmorteza Hosseyni, Aliasghar Jarrahpour: Recent advances in β-lactam synthesis. Organic & Biomolecular Chemistry, 2018, 16. vsk, nro 38, s. 6840–6852. PubMed:30209477 doi:10.1039/c8ob01833b
  • Nanda D. Paul, Andrei Chirila, Hongjian Lu, Peter Zhang, Bas de Bruin: Carbene Radicals in Cobalt(II)–Porphyrin‐Catalysed Carbene Carbonylation Reactions; A Catalytic Approach to Ketenes. Chemistry – a European Journal, 23.9.2013, 19. vsk, nro 38, s. 12953–12958. PubMed:24038393 doi:10.1002/chem.201301731
  • Robert Burns Woodward: Penems and related substances. Philosophical Transactions of the Royal Society, 10.5.1980. PubMed:6109320 doi:10.1098/rstb.1980.0042 Bibcode:1980RSPTB.289..239W
  • Niamh M. O. Boyle, Miriam Carr, Lisa M. Greene, Orla Bergin, Seema M. Mathwan, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents. Journal of Medicinal Chemistry, 16.11.2010. PubMed:21080725 doi:10.1021/jm101115u Artikkelin verkkoversio.
  • Niamh M. O. Boyle, Lisa M. Greene, Orla Bergin, Jean-Baptiste Fichet, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis, evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones. Bioorganic & Medicinal Chemistry, 1.4.2011, 19. vsk, nro 7, s. 2306–2325. PubMed:21397510 doi:10.1016/j.bmc.2011.02.022 Artikkelin verkkoversio.

tcd.ie

tara.tcd.ie

  • Niamh M. O. Boyle, Lisa M. Greene, Orla Bergin, Jean-Baptiste Fichet, Thomas McCabe, David G. Lloyd, Daniela M. Zisterer, Mary J. Meegan: Synthesis, evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones. Bioorganic & Medicinal Chemistry, 1.4.2011, 19. vsk, nro 7, s. 2306–2325. PubMed:21397510 doi:10.1016/j.bmc.2011.02.022 Artikkelin verkkoversio.

ukim.edu.mk

pmf.ukim.edu.mk

uva.nl

pure.uva.nl

web.archive.org

worldcat.org