Baylisova–Hillmanova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Baylisova–Hillmanova reakce" in Czech language version.

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dx.doi.org

  • Ciganek, E. Organic Reactions 1997, 51, 201. DOI:10.1002/0471264180.or051.02
  • Recent Advances in the Baylis−Hillman Reaction and Applications Deevi Basavaiah, Anumolu Jaganmohan Rao, and Tummanapalli Satyanarayana Chemical Reviews, 2003, 103 (3), pp 811–892 2003 (Article) DOI:10.1021/cr010043d
  • Masson, G., Housseman, C. and Zhu, J. (2007), The Enantioselective Morita–Baylis–Hillman Reaction and Its Aza Counterpart. Angewandte Chemie International Edition, 46: 4614–4628. DOI:10.1002/anie.200604366
  • aza-Baylis−Hillman Reaction Valerie Declerck, Jean Martinez and Frederic Lamaty Chemical Reviews, 2009, 109 (1), pp 1–48, 2009 (Review) DOI:10.1021/cr068057c
  • Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry Deevi Basavaiah, Bhavanam Sekhara Reddy and Satpal Singh Badsara Chemical Reviews 2010 110 (9), 5447-5674 DOI:10.1021/cr900291g
  • The Baylis–Hillman reaction: a novel concept for creativity in chemistry Deevi Basavaiah and Gorre Veeraraghavaiah Chemical Society Reviews, 2012, Advance Article DOI:10.1039/C1CS15174F
  • Yves Fort; Marie Christine Berthe; Paul Caubere. The 'Baylis - Hillman Reaction' mechanism and applications revisited. Tetrahedron. 1992, s. 6371–6384. DOI 10.1016/s0040-4020(01)88227-2. 
  • Y. Xiao; Z. Sun; H. Guo; O. Kwon. Chiral Phosphines in Nucleophilic Organocatalysis. Beilstein Journal of Organic Chemistry. 2014, s. 2089–2121. DOI 10.3762/bjoc.10.218. PMID 25246969. 

nih.gov

ncbi.nlm.nih.gov

  • Y. Xiao; Z. Sun; H. Guo; O. Kwon. Chiral Phosphines in Nucleophilic Organocatalysis. Beilstein Journal of Organic Chemistry. 2014, s. 2089–2121. DOI 10.3762/bjoc.10.218. PMID 25246969.