Michaelis–Arbuzov reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Michaelis–Arbuzov reaction" in English language version.

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6doi.org

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1worldcat.org

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1loc.gov

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

Michaelis, A.; Kaehne, R. (1898). "Ueber das Verhalten der Jodalkyle gegen die sogen. Phosphorigsäureester oder O-Phosphine". Berichte. 31: 1048–1055. doi:10.1002/cber.189803101190.
Arbuzov, B. A. (1964). "Michaelis–Arbusow- und Perkow-Reaktionen". Pure Appl. Chem. 9 (2): 307–353. doi:10.1351/pac196409020307. S2CID 93719226.
Bhattacharya, A. K.; Thyagarajan, G. (1981). "Michaelis–Arbuzov rearrangement". Chem. Rev. 81 (4): 415–430. doi:10.1021/cr00044a004.
Gerrard, W.; Green, W. J. (1951). "568. Mechanism of the formation of dialkyl alkylphosphonates". J. Chem. Soc.: 2550. doi:10.1039/jr9510002550.
Kostoudi, Stavroula; Pampalakis, Georgios (2022-03-21). "Improvements, Variations and Biomedical Applications of the Michaelis–Arbuzov Reaction". International Journal of Molecular Sciences. 23 (6): 3395. doi:10.3390/ijms23063395. ISSN 1422-0067. PMC 8955222. PMID 35328816.
Jacobsen, H. I.; Griffin, M. J.; Preis, S.; Jensen, E. V. (1957). "Phosphonic Acids. IV. Preparation and Reactions of β-Ketophosphonate and Enol Phosphate Esters". J. Am. Chem. Soc. 79 (10): 2608. Bibcode:1957JAChS..79.2608J. doi:10.1021/ja01567a067.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Jacobsen, H. I.; Griffin, M. J.; Preis, S.; Jensen, E. V. (1957). "Phosphonic Acids. IV. Preparation and Reactions of β-Ketophosphonate and Enol Phosphate Esters". J. Am. Chem. Soc. 79 (10): 2608. Bibcode:1957JAChS..79.2608J. doi:10.1021/ja01567a067.

loc.gov (Global: 70^th place; English: 63^rd place)

lccn.loc.gov

Almasi, Lucreţia (1971). "The Sulfur–Phosphorus Bond". In Senning, Alexander (ed.). Sulfur in Organic and Inorganic Chemistry. Vol. 1. New York: Marcel Dekker. pp. 51–55. ISBN 0-8247-1615-9. LCCN 70-154612, although note that Almasi identifies the chemoselective axis as hard-softness instead.

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

ncbi.nlm.nih.gov

Kostoudi, Stavroula; Pampalakis, Georgios (2022-03-21). "Improvements, Variations and Biomedical Applications of the Michaelis–Arbuzov Reaction". International Journal of Molecular Sciences. 23 (6): 3395. doi:10.3390/ijms23063395. ISSN 1422-0067. PMC 8955222. PMID 35328816.

pubmed.ncbi.nlm.nih.gov

Kostoudi, Stavroula; Pampalakis, Georgios (2022-03-21). "Improvements, Variations and Biomedical Applications of the Michaelis–Arbuzov Reaction". International Journal of Molecular Sciences. 23 (6): 3395. doi:10.3390/ijms23063395. ISSN 1422-0067. PMC 8955222. PMID 35328816.

orgsyn.org (Global: 2,971^st place; English: 2,826^th place)

Nagata, W.; Wakabayashi, T.; Hayase, Y. (1988). "Diethyl 2-(cyclohexylamino)vinylphosphonate". Organic Syntheses; Collected Volumes, vol. 6, p. 448.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Arbuzov, B. A. (1964). "Michaelis–Arbusow- und Perkow-Reaktionen". Pure Appl. Chem. 9 (2): 307–353. doi:10.1351/pac196409020307. S2CID 93719226.

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

Kostoudi, Stavroula; Pampalakis, Georgios (2022-03-21). "Improvements, Variations and Biomedical Applications of the Michaelis–Arbuzov Reaction". International Journal of Molecular Sciences. 23 (6): 3395. doi:10.3390/ijms23063395. ISSN 1422-0067. PMC 8955222. PMID 35328816.

zenodo.org (Global: 621^st place; English: 380^th place)

Michaelis, A.; Kaehne, R. (1898). "Ueber das Verhalten der Jodalkyle gegen die sogen. Phosphorigsäureester oder O-Phosphine". Berichte. 31: 1048–1055. doi:10.1002/cber.189803101190.

Michaelis–Arbuzov reaction (English Wikipedia)

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

harvard.edu (Global: 18th place; English: 17th place)