Kyánhydrín (Slovak Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kyánhydrín" in Slovak language version.

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acs.org

pubs.acs.org

  • MOWRY, David T.. The Preparation of Nitriles.. Chemical Reviews, 1948-04-01, roč. 42, čís. 2, s. 189–283. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr60132a001. (po anglicky)
  • NORTH, Michael; USANOV, Dmitry L.; YOUNG, Carl. Lewis Acid Catalyzed Asymmetric Cyanohydrin Synthesis. Chemical Reviews, 2008-12-10, roč. 108, čís. 12, s. 5146–5226. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr800255k. (po anglicky)
  • SCHOLL, Matthias; LIM, Chee-Kiang; FU, Gregory C.. Convenient and efficient conversion of aldehydes to acylated cyanohydrins using tributyltin cyanide as catalyst. The Journal of Organic Chemistry, 1995-09, roč. 60, čís. 19, s. 6229–6231. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00124a052. (po anglicky)
  • YONEDA, Ryuji; HARUSAWA, Shinya; KURIHARA, Takushi. Cyano phosphate: an efficient intermediate for the chemoselective conversion of carbonyl compounds to nitriles. The Journal of Organic Chemistry, 1991-03, roč. 56, čís. 5, s. 1827–1832. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00005a031. (po anglicky)

doi.org

dx.doi.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "cyanohydrins". DOI:https://doi.org/10.1351/goldbook
  • MOWRY, David T.. The Preparation of Nitriles.. Chemical Reviews, 1948-04-01, roč. 42, čís. 2, s. 189–283. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr60132a001. (po anglicky)
  • NORTH, Michael; USANOV, Dmitry L.; YOUNG, Carl. Lewis Acid Catalyzed Asymmetric Cyanohydrin Synthesis. Chemical Reviews, 2008-12-10, roč. 108, čís. 12, s. 5146–5226. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr800255k. (po anglicky)
  • LIDY, Werner; SUNDERMEYER, Wolfgang. Spaltungsreaktionen des Trimethylsilylcyanids, eine neue Darstellungsmethode für O ‐(Trimethylsilyl)cyanhydrine. Chemische Berichte, 1973-02, roč. 106, čís. 2, s. 587–593. Dostupné online [cit. 2022-09-19]. ISSN 0009-2940. DOI10.1002/cber.19731060224. (po anglicky)
  • SCHOLL, Matthias; LIM, Chee-Kiang; FU, Gregory C.. Convenient and efficient conversion of aldehydes to acylated cyanohydrins using tributyltin cyanide as catalyst. The Journal of Organic Chemistry, 1995-09, roč. 60, čís. 19, s. 6229–6231. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00124a052. (po anglicky)
  • YONEDA, Ryuji; HARUSAWA, Shinya; KURIHARA, Takushi. Cyano phosphate: an efficient intermediate for the chemoselective conversion of carbonyl compounds to nitriles. The Journal of Organic Chemistry, 1991-03, roč. 56, čís. 5, s. 1827–1832. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00005a031. (po anglicky)
  • JUHL, Martin; PETERSEN, Allan R.; LEE, Ji‐Woong. CO 2 ‐Enabled Cyanohydrin Synthesis and Facile Iterative Homologation Reactions**. Chemistry – A European Journal, 2021-01-04, roč. 27, čís. 1, s. 228–232. Dostupné online [cit. 2022-09-19]. ISSN 0947-6539. DOI10.1002/chem.202003623. (po anglicky)
  • William Bauer, Jr. "Methacrylic Acid and Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. DOI:10.1002/14356007.a16_441. Article Online Posting Date: June 15, 2000
  • Haroutounian, S. A. "Acetone Cyanohydrin" Encyclopedia of Reagents for Organic Synthesis 2001, John Wiley & Sons. DOI:10.1002/047084289X.ra014

iupac.org

goldbook.iupac.org

orgsyn.org

  • Organic Syntheses Procedure [online]. www.orgsyn.org, [cit. 2022-09-19]. Dostupné online. (po anglicky)
  • Organic Syntheses Procedure [online]. www.orgsyn.org, [cit. 2022-09-19]. Dostupné online. (po anglicky)

wiley.com

onlinelibrary.wiley.com

  • LIDY, Werner; SUNDERMEYER, Wolfgang. Spaltungsreaktionen des Trimethylsilylcyanids, eine neue Darstellungsmethode für O ‐(Trimethylsilyl)cyanhydrine. Chemische Berichte, 1973-02, roč. 106, čís. 2, s. 587–593. Dostupné online [cit. 2022-09-19]. ISSN 0009-2940. DOI10.1002/cber.19731060224. (po anglicky)
  • JUHL, Martin; PETERSEN, Allan R.; LEE, Ji‐Woong. CO 2 ‐Enabled Cyanohydrin Synthesis and Facile Iterative Homologation Reactions**. Chemistry – A European Journal, 2021-01-04, roč. 27, čís. 1, s. 228–232. Dostupné online [cit. 2022-09-19]. ISSN 0947-6539. DOI10.1002/chem.202003623. (po anglicky)

worldcat.org

  • MOWRY, David T.. The Preparation of Nitriles.. Chemical Reviews, 1948-04-01, roč. 42, čís. 2, s. 189–283. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr60132a001. (po anglicky)
  • NORTH, Michael; USANOV, Dmitry L.; YOUNG, Carl. Lewis Acid Catalyzed Asymmetric Cyanohydrin Synthesis. Chemical Reviews, 2008-12-10, roč. 108, čís. 12, s. 5146–5226. Dostupné online [cit. 2022-09-19]. ISSN 0009-2665. DOI10.1021/cr800255k. (po anglicky)
  • LIDY, Werner; SUNDERMEYER, Wolfgang. Spaltungsreaktionen des Trimethylsilylcyanids, eine neue Darstellungsmethode für O ‐(Trimethylsilyl)cyanhydrine. Chemische Berichte, 1973-02, roč. 106, čís. 2, s. 587–593. Dostupné online [cit. 2022-09-19]. ISSN 0009-2940. DOI10.1002/cber.19731060224. (po anglicky)
  • SCHOLL, Matthias; LIM, Chee-Kiang; FU, Gregory C.. Convenient and efficient conversion of aldehydes to acylated cyanohydrins using tributyltin cyanide as catalyst. The Journal of Organic Chemistry, 1995-09, roč. 60, čís. 19, s. 6229–6231. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00124a052. (po anglicky)
  • YONEDA, Ryuji; HARUSAWA, Shinya; KURIHARA, Takushi. Cyano phosphate: an efficient intermediate for the chemoselective conversion of carbonyl compounds to nitriles. The Journal of Organic Chemistry, 1991-03, roč. 56, čís. 5, s. 1827–1832. Dostupné online [cit. 2022-09-19]. ISSN 0022-3263. DOI10.1021/jo00005a031. (po anglicky)
  • JUHL, Martin; PETERSEN, Allan R.; LEE, Ji‐Woong. CO 2 ‐Enabled Cyanohydrin Synthesis and Facile Iterative Homologation Reactions**. Chemistry – A European Journal, 2021-01-04, roč. 27, čís. 1, s. 228–232. Dostupné online [cit. 2022-09-19]. ISSN 0947-6539. DOI10.1002/chem.202003623. (po anglicky)