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Triethyl phosphite (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Triethyl phosphite" in English language version.

refsWebsite
Global rank English rank
5doi.org
2nd place
2nd place
2nih.gov
4th place
4th place

doi.org (Global: 2nd place; English: 2nd place)

  • Ford-Moore, A. H.; Perry, B. J. (1951). "Triethyl Phosphite". Org. Synth. 31: 111. doi:10.15227/orgsyn.031.0111.
  • Piscopio, Anthony D.; Shakya, Sagar (2005). "Triethyl Phosphite". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rt224.pub2. ISBN 0-471-93623-5.
  • Gardner, J. N.; Carlon, F. E.; Gnoj, O. (1968). "One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones". The Journal of Organic Chemistry. 33 (8): 3294–3297. doi:10.1021/jo01272a055. PMID 5742870.
  • Liang, Yu-Feng; Jiao, Ning (2014). "Highly Efficient C–H Hydroxylation of Carbonyl Compounds with Oxygen under Mild Conditions". Angewandte Chemie International Edition. 53 (2): 548–552. doi:10.1002/anie.201308698. PMID 24281892.
  • Ittel, Steven D. (1990). "Complexes of Nickel(0)". Inorganic Syntheses. Inorganic Syntheses. Vol. 28. pp. 98–104. doi:10.1002/9780470132593.ch26. ISBN 978-0-470-13259-3.

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

  • Gardner, J. N.; Carlon, F. E.; Gnoj, O. (1968). "One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones". The Journal of Organic Chemistry. 33 (8): 3294–3297. doi:10.1021/jo01272a055. PMID 5742870.
  • Liang, Yu-Feng; Jiao, Ning (2014). "Highly Efficient C–H Hydroxylation of Carbonyl Compounds with Oxygen under Mild Conditions". Angewandte Chemie International Edition. 53 (2): 548–552. doi:10.1002/anie.201308698. PMID 24281892.