Swernova oxidace (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Swernova oxidace" in Czech language version.

refsWebsite
Global rank Czech rank
2nd place
4th place
2,971st place
1,658th place

doi.org

dx.doi.org

  • Omura, K.; Swern, D.. Oxidation of alcohols by "activated" dimethyl sulfoxide. A preparative, steric and mechanistic study. Tetrahedron. 1978, s. 1651–1660. DOI 10.1016/0040-4020(78)80197-5. 
  • Mancuso, A. J.; Brownfain, D. S.; Swern, D.. Structure of the dimethyl sulfoxide-oxalyl chloride reaction product. Oxidation of heteroaromatic and diverse alcohols to carbonyl compounds. J. Org. Chem.. 1979, s. 4148–4150. DOI 10.1021/jo01337a028. 
  • Mancuso, A. J.; Huang, S.-L.; Swern, D.. Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride. J. Org. Chem.. 1978, s. 2480–2482. DOI 10.1021/jo00406a041. 
  • Mancuso, A. J.; Swern, D.. Activated dimethyl sulfoxide: Useful reagents for synthesis. Synthesis. 1981, s. 165–185. DOI 10.1055/s-1981-29377. 
  • Tidwell, T. T. Oxidation of alcohols to carbonyl compounds via alkoxysulfonium ylides: The Moffatt, Swern, and related oxidations. Org. React.. 1990, s. 297–572. DOI 10.1002/0471264180.or039.03. 
  • Tidwell, T. T. Oxidation of alcohols by activated dimethyl sulfoxide and related reactions: An update. Synthesis. 1990, s. 857–870. DOI 10.1055/s-1990-27036. 
  • De Luca Lidia. A Mild and Efficient Alternative to the Classical Swern Oxidation. The Journal of Organic Chemistry. S. 7907–7909. DOI 10.1021/jo015935s. 

orgsyn.org

  • DONDONI, A.; PERRONE, D. Synthesis of 1,1-Dimethyl Ethyl-(S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate by Oxidation of the Alcohol. Org. Synth.. 2004. Dostupné online. ; Coll. Vol.. S. 320. 
  • BISHOP, R. 9-Thiabicyclo[3.3.1]nonane-2,6-dione. Org. Synth.. 1998. Dostupné online. ; Coll. Vol.. S. 692. 
  • LEOPOLD, E. J. Selective hydroboration of a 1,3,7-triene: Homogeraniol. Org. Synth.. 1990. Dostupné online. ; Coll. Vol.. S. 258.