Phosphite ester (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Phosphite ester" in English language version.

refsWebsite

Global rank English rank

11doi.org

2^nd place

4nih.gov

4^th place

1orgsyn.org

2,971^st place

2,826^th place

1uva.nl

3,518^th place

2,652^nd place

1worldcat.org

5^th place

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

Malowan, John E. (1953). "Diethyl phosphite". Inorganic Syntheses. Inorganic Syntheses. Vol. 4. pp. 58–60. doi:10.1002/9780470132357.ch19. ISBN 9780470132357. {{cite book}}: ISBN / Date incompatibility (help)
Gerrard, W.; Whitbread, E. G. G. (1952). "165. Interaction of hydrogen halides and n-butyl phosphites". Journal of the Chemical Society (Resumed): 914. doi:10.1039/JR9520000914.
Mao, Mengmei; Zhang, Le; Yao, Hanlin; Wan, Li; Xin, Zhong (28 April 2020). "Development and Scale-up of the Rapid Synthesis of Triphenyl Phosphites in Continuous Flow". ACS Omega. 5 (16): 9503–9509. doi:10.1021/acsomega.0c00716. PMC 7191834. PMID 32363302.
Hoffmann, Friedrich W.; Ess, Richard J.; Usingef, Robert P. (November 1956). "The Transesterification of Trialkyl Phosphites with Aliphatic Alcohols". Journal of the American Chemical Society. 78 (22): 5817–5821. doi:10.1021/ja01603a026.
Rainer Wolf; Bansi Lal Kaul (2000). "Plastics, Additives". Ullmann's Encyclopedia Of Industrial Chemistry. doi:10.1002/14356007.a20_459. ISBN 3527306730.
J. N. Gardner; F. E. Carlon & O. Gnoj (1968). "One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones". J. Org. Chem. 33 (8): 3294–3297. doi:10.1021/jo01272a055. PMID 5742870.
Cuny, Gregory D.; Buchwald, Stephen L. (1993). "Practical, High-Yield, Regioselective, Rhodium-Catalyzed Hydroformylation of Functionalized α-olefins". Journal of the American Chemical Society. 115 (5): 2066–2068. doi:10.1021/ja00058a079.
Van Rooy, Annemiek; Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M.; Goubitz, Kees; Fraanje, Jan; Veldman, Nora; Spek, Anthony L. (1996). "Bulky Diphosphite-Modified Rhodium Catalysts: Hydroformylation and Characterization". Organometallics. 15 (2): 835–847. doi:10.1021/OM950549K.
Aitor Gual; Cyril Godard; Verónica de la Fuente; Sergio Castillón (2012). "Design and Synthesis of Phosphite Ligands for Homogeneous Catalysis". In Paul C. J. Kamer; Piet W. N. M. van Leeuwen (eds.). Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis. John Wiley & Sons. pp. 81–131. doi:10.1002/9781118299715.ch3. ISBN 9781118299715.
Guthrie, J. Peter (1979). "Tautomerization Equilibria for Phosphorous Acid and its Ethyl Esters, Free Energies of Formation of Phosphorous and Phosphonic Acids and their Ethyl Esters, and p Ka Values for Ionization of the P—H Bond in Phosphonic Acid and Phosphonic Esters". Canadian Journal of Chemistry. 57 (2): 236–239. doi:10.1139/v79-039.
Janesko, Benjamin G.; Fisher, Henry C.; Bridle, Mark J.; Montchamp, Jean-Luc (2015-09-29). "P(═O)H to P–OH Tautomerism: A Theoretical and Experimental Study". The Journal of Organic Chemistry. 80 (20). American Chemical Society (ACS): 10025–10032. doi:10.1021/acs.joc.5b01618. ISSN 0022-3263. PMID 26372089.

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

pubmed.ncbi.nlm.nih.gov

Mao, Mengmei; Zhang, Le; Yao, Hanlin; Wan, Li; Xin, Zhong (28 April 2020). "Development and Scale-up of the Rapid Synthesis of Triphenyl Phosphites in Continuous Flow". ACS Omega. 5 (16): 9503–9509. doi:10.1021/acsomega.0c00716. PMC 7191834. PMID 32363302.
J. N. Gardner; F. E. Carlon & O. Gnoj (1968). "One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones". J. Org. Chem. 33 (8): 3294–3297. doi:10.1021/jo01272a055. PMID 5742870.
Janesko, Benjamin G.; Fisher, Henry C.; Bridle, Mark J.; Montchamp, Jean-Luc (2015-09-29). "P(═O)H to P–OH Tautomerism: A Theoretical and Experimental Study". The Journal of Organic Chemistry. 80 (20). American Chemical Society (ACS): 10025–10032. doi:10.1021/acs.joc.5b01618. ISSN 0022-3263. PMID 26372089.

ncbi.nlm.nih.gov

Mao, Mengmei; Zhang, Le; Yao, Hanlin; Wan, Li; Xin, Zhong (28 April 2020). "Development and Scale-up of the Rapid Synthesis of Triphenyl Phosphites in Continuous Flow". ACS Omega. 5 (16): 9503–9509. doi:10.1021/acsomega.0c00716. PMC 7191834. PMID 32363302.

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

A. H. Ford-Moore & B. J. Perry (1963). "Triethyl Phosphite". Organic Syntheses; Collected Volumes, vol. 4, p. 955.

uva.nl (Global: 3,518^th place; English: 2,652^nd place)

dare.uva.nl

Van Rooy, Annemiek; Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M.; Goubitz, Kees; Fraanje, Jan; Veldman, Nora; Spek, Anthony L. (1996). "Bulky Diphosphite-Modified Rhodium Catalysts: Hydroformylation and Characterization". Organometallics. 15 (2): 835–847. doi:10.1021/OM950549K.

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

search.worldcat.org

Janesko, Benjamin G.; Fisher, Henry C.; Bridle, Mark J.; Montchamp, Jean-Luc (2015-09-29). "P(═O)H to P–OH Tautomerism: A Theoretical and Experimental Study". The Journal of Organic Chemistry. 80 (20). American Chemical Society (ACS): 10025–10032. doi:10.1021/acs.joc.5b01618. ISSN 0022-3263. PMID 26372089.

Phosphite ester (English Wikipedia)

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

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