Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. sid. 375. doi:10.1039/9781849733069-00372. ISBN 978-0-85404-182-4. ”The name carbodiimide, for HN=C=NH, is retained but only for general nomenclature; no substitution of any kind is allowed. The systematic name, methanediimine, is the preferred IUPAC name.”
Andrew Williams; Ibrahim T. Ibrahim (1981). ”Carbodiimide Chemistry: recent Advances”. Chem. Rev. 81 (6): sid. 589–636. doi:10.1021/cr00046a004.
T. W. Campbell; J. J. Monagle (1963). ”Diphenylcarbodiimide”. Org. Synth. 43: sid. 31. doi:10.15227/orgsyn.043.0031.
Irngartinger, H.; Jäger, H.-U. (1978). ”Kristall- und Molekularstrukturen von zwei Carbodiimiden: Bis(diphenylmethyl)carbodiimid und Bis(p-methoxyphenyl)-carbodiimid”. Acta Crystallographica Section B: Structural Crystallography and Crystal Chemistry 34 (11): sid. 3262–3265. doi:10.1107/S0567740878010626.
Vincent, A. T.; Wheatley, P. J. (1972). ”Crystal Structure of Bis-p-nitrophenylcarbodiimide, O2N·C6H4·N:C:N·C6H4·NO2”. Journal of the Chemical Society, Perkin Transactions 2 (11): sid. 1567–1571. doi:10.1039/P29720001567.
Frederick Kurzer; K. Douraghi-Zadeh (1967). ”Advances in the Chemistry of Carbodiimides”. Chem. Rev. 67 (2): sid. ee107–152. doi:10.1021/cr60246a001. PMID 4859920.
John C. Sheehan; Philip A. Cruickshank (1968). ”1-Ethyl-3-(3-Dimethylamino)propylcarbodiimide Hydrochloride and Methiodide”. Org. Synth. 48: sid. 83. doi:10.15227/orgsyn.048.0083.
Arnab K. Maity; Skye Fortier; Leonel Griego; Alejandro J. Metta-Magaña (2014). ”Synthesis of a "Super Bulky" Guanidinate Possessing an Expandable Coordination Pocket”. Inorg. Chem. 53 (15): sid. 8155–8164. doi:10.1021/ic501219q. PMID 25029088.
Monagle, J. J. (1962). ”Carbodiimides. III. Conversion of Isocyanates to Carbodiimides. Catalyst Studies”. J. Org. Chem. 27 (11): sid. 3851–3855. doi:10.1021/jo01058a022.
Li, Zhen; Mayer, Robert J.; Ofial, Armin R.; Mayr, Herbert (2020-04-27). ”From Carbodiimides to Carbon Dioxide: Quantification of the Electrophilic Reactivities of Heteroallenes”. Journal of the American Chemical Society 142 (18): sid. 8383–8402. doi:10.1021/jacs.0c01960. PMID 32338511.
Tidwell, T. T. (1990). ”Oxidation of Alcohols by Activated Dimethyl Sulfoxide and Related Reactions: An Update”. Synthesis 1990 (10): sid. 857–870. doi:10.1055/s-1990-27036.
Hesselmans, L. C. J.; Derksen, A. J.; van den Goorbergh, J. A. M. (2006). ”Polycarbodiimide crosslinkers”. Progress in Organic Coatings 55 (2): sid. 142–148. doi:10.1016/j.porgcoat.2005.08.011. ISSN0300-9440.
Posthumus, W.; Derksen, A. J.; van den Goorbergh, J. A. M.; Hesselmans, L. C. J. (2007). ”Crosslinking by polycarbodiimides”. Progress in Organic Coatings 58 (2–3): sid. 231–236. doi:10.1016/j.porgcoat.2006.09.031. ISSN0300-9440.
Frederick Kurzer; K. Douraghi-Zadeh (1967). ”Advances in the Chemistry of Carbodiimides”. Chem. Rev. 67 (2): sid. ee107–152. doi:10.1021/cr60246a001. PMID 4859920.
Arnab K. Maity; Skye Fortier; Leonel Griego; Alejandro J. Metta-Magaña (2014). ”Synthesis of a "Super Bulky" Guanidinate Possessing an Expandable Coordination Pocket”. Inorg. Chem. 53 (15): sid. 8155–8164. doi:10.1021/ic501219q. PMID 25029088.
Li, Zhen; Mayer, Robert J.; Ofial, Armin R.; Mayr, Herbert (2020-04-27). ”From Carbodiimides to Carbon Dioxide: Quantification of the Electrophilic Reactivities of Heteroallenes”. Journal of the American Chemical Society 142 (18): sid. 8383–8402. doi:10.1021/jacs.0c01960. PMID 32338511.
Hesselmans, L. C. J.; Derksen, A. J.; van den Goorbergh, J. A. M. (2006). ”Polycarbodiimide crosslinkers”. Progress in Organic Coatings 55 (2): sid. 142–148. doi:10.1016/j.porgcoat.2005.08.011. ISSN0300-9440.
Posthumus, W.; Derksen, A. J.; van den Goorbergh, J. A. M.; Hesselmans, L. C. J. (2007). ”Crosslinking by polycarbodiimides”. Progress in Organic Coatings 58 (2–3): sid. 231–236. doi:10.1016/j.porgcoat.2006.09.031. ISSN0300-9440.