Fosfonio (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fosfonio" in Italian language version.

refsWebsite

Global rank Italian rank

2^nd place

7^th place

1,248^th place

1,065^th place

4^th place

9^th place

538^th place

93^rd place

1,735^th place

3,587^th place

low place

low place

2,020^th place

1,112^th place

acs.org

pubs.acs.org

(EN) G. A. Wiley; R. L. Hershkowitz; B. M. Rein; B. C. Chung, Studies in Organophosphorus Chemistry. I. Conversion of Alcohols and Phenols to Halides by Tertiary Phosphine Dihalides, in J. Am. Chem. Soc., vol. 86, n. 5, 1964, pp. 964-965, DOI:10.1021/ja01059a073.
(EN) Jennings E. V.; Nikitin K.; Ortin Y.; Gilheany D. G., Degenerate Nucleophilic Substitution in Phosphonium Salts, in J. Am. Chem. Soc., vol. 136, n. 46, 2014, pp. 16217–16226, DOI:10.1021/ja507433g, PMID 25384344.

arkat-usa.org

(EN) Paola Hernández; Alicia Merlino; Alejandra Gerpe; Williams Porcal; Oscar E. Piro; Mercedes González; Hugo Cerecetto, One-pot synthesis of benzyltriphenylphosphonium acetates from the corresponding activated benzyl alcohols (PDF), in Arkivoc, vol. 11, 2006, pp. 128-136.

doi.org

dx.doi.org

(EN) G. A. Wiley; R. L. Hershkowitz; B. M. Rein; B. C. Chung, Studies in Organophosphorus Chemistry. I. Conversion of Alcohols and Phenols to Halides by Tertiary Phosphine Dihalides, in J. Am. Chem. Soc., vol. 86, n. 5, 1964, pp. 964-965, DOI:10.1021/ja01059a073.
(EN) Stephen M. Godfrey; Charles A. McAuliffe; Robin G. Pritchard; Joanne M. Sheffield, Structural dependence of the reagent Ph₃PCl₂ on the nature of the solvent, both in the solid state and in solution; X-ray Crystal structure of trigonal bipyramidal Ph₃PCl₂, the first structurally characterised five-coordinate R₃PCl₂ compound, in Chem. Commun., vol. 1998, n. 8, 1998, pp. 921-922, DOI:10.1039/a800820e.
(EN) Jennings E. V.; Nikitin K.; Ortin Y.; Gilheany D. G., Degenerate Nucleophilic Substitution in Phosphonium Salts, in J. Am. Chem. Soc., vol. 136, n. 46, 2014, pp. 16217–16226, DOI:10.1021/ja507433g, PMID 25384344.

iupac.org

old.iupac.org

(EN) Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). 6ed, Cambridge (UK), RSC/IUPAC (2005). ISBN 0-85404-438-8. Versione elettronica.

nih.gov

pubchem.ncbi.nlm.nih.gov

(EN) PubChem Compound, Phosphonium - Compound Summary, su pubchem.ncbi.nlm.nih.gov, National Center for Biotechnology Information, 30 Giugno 2019. URL consultato il 9 Luglio 2019.

ncbi.nlm.nih.gov

(EN) Jennings E. V.; Nikitin K.; Ortin Y.; Gilheany D. G., Degenerate Nucleophilic Substitution in Phosphonium Salts, in J. Am. Chem. Soc., vol. 136, n. 46, 2014, pp. 16217–16226, DOI:10.1021/ja507433g, PMID 25384344.

qmul.ac.uk

sbcs.qmul.ac.uk

(EN) IUPAC CIAAW., Atomic weights of the elements 2017, su Queen Mary University of London.

rsc.org

pubs.rsc.org

(EN) Stephen M. Godfrey; Charles A. McAuliffe; Robin G. Pritchard; Joanne M. Sheffield, Structural dependence of the reagent Ph₃PCl₂ on the nature of the solvent, both in the solid state and in solution; X-ray Crystal structure of trigonal bipyramidal Ph₃PCl₂, the first structurally characterised five-coordinate R₃PCl₂ compound, in Chem. Commun., vol. 1998, n. 8, 1998, pp. 921-922, DOI:10.1039/a800820e.