Salicylaldehyde (English Wikipedia)

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

refsWebsite

Global rank English rank

11doi.org

2^nd place

1sigmaaldrich.com

924^th place

2,352^nd place

1nih.gov

4^th place

1springer.com

274^th place

309^th place

1orgsyn.org

2,971^st place

2,826^th place

1zenodo.org

621^st place

380^th place

doi.org

"Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 652. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
Maliverney, Christian; Mulhauser, Michel (2000). "Hydroxybenzaldehydes". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.0825041813011209.a01. ISBN 978-0-471-48494-3.
Trond Vidar Hansen; Lars Skattebøl (2005). "Ortho-Formylation of Phenols; Preparation of 3-Bromosalicylaldehyde". Organic Syntheses. 82: 64. doi:10.15227/orgsyn.089.0220.
Brühne, F.; Wright, E. "Benzaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_463.pub2. ISBN 978-3527306732.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)
Janeš, D.; Kreft, S. (2008). "Salicylaldehyde is a characteristic aroma component of buckwheat groats". Food Chemistry. 109 (2): 293–298. doi:10.1016/j.foodchem.2007.12.032. PMID 26003350.
Burgstahler, A. W.; Worden, L. R. (1966). "Coumarone". Organic Syntheses. 46: 28. doi:10.15227/orgsyn.046.0028{{cite journal}}: CS1 maint: multiple names: authors list (link).
Stoermer, R. (1900). "Synthesen und Abbaureactionen in der Cumaronreihe". Liebig's Annalen der Chemie. 312 (3): 237–336. doi:10.1002/jlac.19003120302.
Horning, E. C.; Horning, M. G.; Dimmig, D. A. (1948). "3-Carbethoxycoumarin". Organic Syntheses. 28: 24. doi:10.15227/orgsyn.028.0024{{cite journal}}: CS1 maint: multiple names: authors list (link).
Schoustra, S.K.; Asadi, V.; Zuilhof, H.; Smulders, M.M.J. (2023). "Internal hydrogen bonding of imines to control and enhance the dynamic mechanical properties of covalent adaptable networks". European Polymer Journal. 195: 112209. doi:10.1016/j.eurpolymj.2023.112209.
Metzler, C.M.; Cahill, A.; Metzler, D.E. (1980). "Equilibriums and absorption spectra of Schiff bases". J. Am. Chem. Soc. 102 (19): 6075–6082. doi:10.1021/ja00539a017.
Kandambeth, S.; Shinde, D.B; Panda, M.K.; Lukose, B.; Heine, T.; Banerjee, R. (2013). "Enhancement of Chemical Stability and Crystallinity in Porphyrin-Containing Covalent Organic Frameworks by Intramolecular Hydrogen Bonds". Angew. Chem. Int. Ed. 52 (49): 13052–13056. doi:10.1002/anie.201306775.

nih.gov

pubmed.ncbi.nlm.nih.gov

Janeš, D.; Kreft, S. (2008). "Salicylaldehyde is a characteristic aroma component of buckwheat groats". Food Chemistry. 109 (2): 293–298. doi:10.1016/j.foodchem.2007.12.032. PMID 26003350.

orgsyn.org

Dakin, H. D. (1923). "Catechol" (PDF). Organic Syntheses. 3: 28; Collected Volumes, vol. 1, p. 149.

sigmaaldrich.com

Sigma-Aldrich Co., Salicylaldehyde. Retrieved on 2018-05-24.

springer.com

link.springer.com

Pauls, G., Becker, T., et al. (2016). Two Defensive Lines in Juvenile Leaf Beetles; Esters of 3-nitropropionic Acid in the Hemolymph and Aposematic Warning. Journal of Chemical Ecology 42 (3) 240-248.

zenodo.org

Stoermer, R. (1900). "Synthesen und Abbaureactionen in der Cumaronreihe". Liebig's Annalen der Chemie. 312 (3): 237–336. doi:10.1002/jlac.19003120302.