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Newman–Kwart rearrangement (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Newman–Kwart rearrangement" in English language version.

refsWebsite
Global rank English rank
9doi.org
2nd place
2nd place
4nih.gov
4th place
4th place
2worldcat.org
5th place
5th place
1cdnsciencepub.com
low place
low place
1acs.org
1,248th place
1,104th place

acs.org

pubs.acs.org

cdnsciencepub.com

doi.org

  • Zonta, C.; De Lucchi, O.; Volpicelli, R.; Cotarca, L. (2007). Thione–Thiol Rearrangement: Miyazaki–Newman–Kwart Rearrangement and Others. Topics in Current Chemistry. Vol. 275. Springer Berlin / Heidelberg. pp. 131–161. doi:10.1007/128_065. ISBN 978-3-540-68099-4. ISSN 0340-1022. PMID 23605512.
  • Harvey, J. N.; Jover, J.; Lloyd-Jones, G. C.; Moseley, J. D.; Murray, P. M.; Renny, J. S. (2009). "The Newman–Kwart Rearrangement of O-Aryl Thiocarbamates: Substantial Reduction in Reaction Temperatures through Palladium Catalysis". Angew. Chem. Int. Ed. 48 (41): 7612–7615. doi:10.1002/anie.200903908. PMID 19746383.
  • Lloyd-Jones, G. C.; Moseley, J. D.; Renny, J. S. (2008). "Mechanism and Application of the Newman-Kwart O→S Rearrangement of O-Aryl Thiocarbamates". Synthesis. 2008 (5): 661–689. doi:10.1055/s-2008-1032179.
  • Newman, M. S.; Karnes, H. A. (1966). "The Conversion of Phenols to Thiophenols via Dialkylthiocarbamates". J. Org. Chem. 31 (12): 3980–3984. doi:10.1021/jo01350a023.
  • Kwart, H.; Evans, E. R. (1966). "The Vapor Phase Rearrangement of Thioncarbonates and Thioncarbamates". J. Org. Chem. 31 (2): 410–413. doi:10.1021/jo01340a015.
  • Burns, Matthew; Lloyd-Jones, G. C.; Moseley, J. D.; Renny, J. S. (2010). "The Molecularity of the Newman−Kwart Rearrangement". J. Org. Chem. 75 (19): 6347–6353. doi:10.1021/jo1014382. PMID 20812755.
  • Jacobsen, Heiko; Donahue, James P. (2011-02-05). "Expanding the scope of the Newman–Kwart rearrangement — A computational assessment". Canadian Journal of Chemistry. 84 (11): 1567–1574. doi:10.1139/v06-161.
  • Perkowski, Andrew J.; Cruz, Cole L.; Nicewicz, David A. (2015-12-23). "Ambient-Temperature Newman–Kwart Rearrangement Mediated by Organic Photoredox Catalysis". Journal of the American Chemical Society. 137 (50): 15684–15687. doi:10.1021/jacs.5b11800. ISSN 0002-7863. PMID 26645387.
  • Melvin S. Newman; Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Zonta, C.; De Lucchi, O.; Volpicelli, R.; Cotarca, L. (2007). Thione–Thiol Rearrangement: Miyazaki–Newman–Kwart Rearrangement and Others. Topics in Current Chemistry. Vol. 275. Springer Berlin / Heidelberg. pp. 131–161. doi:10.1007/128_065. ISBN 978-3-540-68099-4. ISSN 0340-1022. PMID 23605512.
  • Harvey, J. N.; Jover, J.; Lloyd-Jones, G. C.; Moseley, J. D.; Murray, P. M.; Renny, J. S. (2009). "The Newman–Kwart Rearrangement of O-Aryl Thiocarbamates: Substantial Reduction in Reaction Temperatures through Palladium Catalysis". Angew. Chem. Int. Ed. 48 (41): 7612–7615. doi:10.1002/anie.200903908. PMID 19746383.
  • Burns, Matthew; Lloyd-Jones, G. C.; Moseley, J. D.; Renny, J. S. (2010). "The Molecularity of the Newman−Kwart Rearrangement". J. Org. Chem. 75 (19): 6347–6353. doi:10.1021/jo1014382. PMID 20812755.
  • Perkowski, Andrew J.; Cruz, Cole L.; Nicewicz, David A. (2015-12-23). "Ambient-Temperature Newman–Kwart Rearrangement Mediated by Organic Photoredox Catalysis". Journal of the American Chemical Society. 137 (50): 15684–15687. doi:10.1021/jacs.5b11800. ISSN 0002-7863. PMID 26645387.

worldcat.org

search.worldcat.org

  • Zonta, C.; De Lucchi, O.; Volpicelli, R.; Cotarca, L. (2007). Thione–Thiol Rearrangement: Miyazaki–Newman–Kwart Rearrangement and Others. Topics in Current Chemistry. Vol. 275. Springer Berlin / Heidelberg. pp. 131–161. doi:10.1007/128_065. ISBN 978-3-540-68099-4. ISSN 0340-1022. PMID 23605512.
  • Perkowski, Andrew J.; Cruz, Cole L.; Nicewicz, David A. (2015-12-23). "Ambient-Temperature Newman–Kwart Rearrangement Mediated by Organic Photoredox Catalysis". Journal of the American Chemical Society. 137 (50): 15684–15687. doi:10.1021/jacs.5b11800. ISSN 0002-7863. PMID 26645387.