Danishefského dien (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Danishefského dien" in Czech language version.

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beilstein-journals.org

bjoc.beilstein-journals.org

doi.org

dx.doi.org

  • Samuel J. Danishefsky; Kitahara, T. Useful diene for the Diels-Alder reaction. J. Am. Chem. Soc. 1974, 96, 7807-7808. DOI:10.1021/ja00832a031
  • Acid-Free Aza Diels−Alder Reaction of Danishefsky's Diene with Imines Yu Yuan, Xin Li, and Kuiling Ding: Organic Letters 2002 4 (19), 3309-3311 DOI:10.1021/ol0265822
  • Alkaline salt-catalyzed aza Diels–Alder reactions of Danishefsky’s diene with imines in water under neutral conditions Catherine Loncaric, Kei Manabea and Shū Kobayashi Chem. Commun., 2003, 574-575 DOI:10.1039/B300880K
  • Exo selective Diels–Alder reaction of nitroolefins with Danishefsky's diene Manabu Node, Kiyoharu Nishide, Hitoshi Imazato, Ryuichi Kurosaki, Takehisa Inoue and Takao Ikariya Chem. Commun., 1996, 2559-2560 DOI:10.1039/CC9960002559
  • Total asymmetric synthesis of the putative structure of the cytotoxic diterpenoid (−)-sclerophytin a and of the authentic natural sclerophytins A and B. Bernardelli P, Moradei OM, Friedrich D, Yang J, Gallou F, Dyck BP, Doskotch RW, Lange T, Paquette LA. J Am Chem Soc. 2001 Sep 19;123(37):9021-32. DOI:10.1021/ja011285y
  • A straightforward stereoselective synthesis of D- and L-5-hydroxy-4-hydroxymethyl-2-cyclohexenylguanine. Wang J, Morral J, Hendrix C, Herdewijn P.J Org Chem. 2001 Dec 14;66(25):8478-82. DOI:10.1021/jo015924z
  • Chiral hetero Diels-Alder products by enantioselective and diastereoselective zirconium catalysis. Scope, limitation, mechanism, and application to the concise synthesis of (+)-Prelactone C and (+)-9-deoxygoniopypyrone. Yamashita Y, Saito S, Ishitani H, Kobayashi S.J Am Chem Soc. 2003 Apr 2;125(13):3793-8. DOI:10.1021/ja028186k
  • Enantioselective catalysis of hetero Diels-Alder reaction and diethylzinc addition using a single catalyst. Du H, Ding K.Org Lett. 2003 Apr 3;5(7):1091-3. DOI:10.1021/ol034143c
  • Asymmetric hetero Diels-Alder reactions of Danishefsky's diene and glyoxylate esters catalyzed by chiral bisoxazoline derived catalysts Arun K. Ghosh, Packiarajan Mathivanan, John Cappiello, K. Krishnan Tetrahedron: Asymmetry Volume 7, Issue 8, August 1996, Pages 2165–2168 DOI:10.1016/0957-4166(96)00261-3
  • Asymmetric Hetero-Diels–Alder Reaction of Danishefsky’s Dienes with α-Carbonyl Esters Catalyzed by an Indium(III)–PyBox Complex Bei Zhao and Teck-Peng Loh Organic Letters 2013 15 (12), 2914-2917 DOI:10.1021/ol400841s
  • A Highly Enantioselective Hetero-Diels−Alder Reaction of Aldehydes with Danishefsky's Diene Catalyzed by Chiral Titanium(IV) 5,5‘,6,6‘,7,7‘,8,8‘-Octahydro-1,1‘-bi-2-naphthol Complexes Bin Wang, Xiaoming Feng, Yaozong Huang, Hui Liu, Xin Cui and Yaozhong Jiang The Journal of Organic Chemistry 2002 67 (7), 2175-2182 DOI:10.1021/jo016240u
  • Zheng, J., Lin, L., Fu, K., Zhang, Y., Liu, X. and Feng, X. (2014), Asymmetric Hetero-Diels–Alder Reaction of Danishefsky’s Diene with α-Ketoesters and Isatins Catalyzed by a Chiral N,N′-Dioxide/Magnesium(II) Complex. Chem. Eur. J., 20: 14493–14498. DOI:10.1002/chem.201404144
  • Difluorinated Danishefsky's diene: a versatile C(4) building block for the fluorinated six-membered rings. Amii H, Kobayashi T, Terasawa H, Uneyama K. Org Lett. 2001 Oct 4;3(20):3103-5. DOI:10.1021/ol0163631

merck.de

assets.chemportals.merck.de

nih.gov

ncbi.nlm.nih.gov

  • Development of an unusually highly enantioselective hetero-Diels-Alder reaction of benzaldehyde with activated dienes catalyzed by hypercoordinating chiral aluminum complexes Simonsen KB1, Svenstrup N, Roberson M, Jorgensen KA. Chemistry. 2000 Jan;6(1):123-8. PMID 10747395
  • Catalytic enantioselective aza-Diels-alder reactions of imines--an approach to optically active nonproteinogenic alpha-amino acids Yao S, Saaby S, Hazell RG, Jorgensen KA. Chemistry. 2000 Jul 3;6(13):2435-48. PMID 10939745
  • Total syntheses of the Securinega alkaloids (+)-14,15-dihydronorsecurinine, (−)-norsecurinine, and phyllanthine. Han G, LaPorte MG, Folmer JJ, Werner KM, Weinreb SM. J Org Chem. 2000 Oct 6;65(20):6293-306. PMID 11052071
  • Racemic and asymmetric Diels-Alder reactions of 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes. Janey JM, Iwama T, Kozmin SA, Rawal VH.J Org Chem. 2000 Dec 29;65(26):9059-68.PMID 11149852

pubchem.ncbi.nlm.nih.gov

  • 1-Methoxy-3-trimethylsiloxy-1,3-butadiene. pubchem.ncbi.nlm.nih.gov [online]. PubChem [cit. 2021-05-24]. Dostupné online. (anglicky) 

orgsyn.org

  • Preparation and Diels-Alder Reaction of a Highly Nuclerophilic Diene. Org. Synth., Coll. Vol. 7, p.312 (1990); Vol. 61, p.147 (1983). Link Archivováno 17. 2. 2012 na Wayback Machine.

web.archive.org