Kyselina pivalová (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kyselina pivalová" in Czech language version.

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Wilhelm Riemenschneider. Ullmann's Encyclopedia of Industrial Chemistry. [s.l.]: [s.n.], 2000. ISBN 3527306730. DOI 10.1002/14356007.a05_235. Kapitola Carboxylic Acids, Aliphatic.
S. V. PUNTAMBEKER; E. A. ZOELLNER; L. T. SANDBORN; E. W. BOUSQUET. Trimethylacetic acid from tert.- Butyl Chloride. Org. Synth.. 1941. Dostupné online. DOI 10.15227/orgsyn.008.0104. ; Coll. Vol.. S. 524.
L. T. SANDBORN; E. W. BOUSQUET. Trimethylacetic acid from Pinacolone. Org. Synth.. 1941. Dostupné online. DOI 10.15227/orgsyn.008.0104. ; Coll. Vol.. S. 524.
Marc Lafrance; Keith Fagnou. Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design. Journal of the American Chemical Society. 2006-12-27, s. 16496–16497. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja067144j. PMID 17177387.
Dongbing Zhao; Weida Wang; Shuang Lian; Fei Yang; Jingbo Lan; Jingsong You. Phosphine-Free, Palladium-Catalyzed Arylation of Heterocycles through C−H Bond Activation with Pivalic Acid as a Cocatalyst. Chemistry – A European Journal. 2009-01-26, s. 16496–16497. Dostupné online. ISSN 0947-6539. DOI 10.1002/chem.200802001. Archivováno 31. 10. 2021 na Wayback Machine.
Morris J. Robins; S. D. Hawrelak; Tadashi Kanai; Jan Marcus Siefert; Rudolf Mengel. Nucleic acid related compounds. 30. Transformations of adenosine to the first 2',3'-aziridine-fused nucleosides, 9-(2,3-epimino-2,3-dideoxy-.beta.-D-ribofuranosyl)adenine and 9-(2,3-epimino-2,3-dideoxy-.beta.-D-lyxofuranosyl)adenine. The Journal of Organic Chemistry. 1979, s. 1317–1322. DOI 10.1021/jo01322a026.
C. A. A. Van Boeckel; J. H. Van Boom. Synthesis of glucosylphosphatidylglycerol via a phosphotriester intermediate. Tetrahedron Letters. 1979, s. 3561–3564. DOI 10.1016/S0040-4039(01)95462-0.
B. E. Griffin; M. Jarman; C. B. Reese. The Synthesis of oligoribonucleotides—IV. Tetrahedron. 1968, s. 639–662. DOI 10.1016/0040-4020(68)88015-9. PMID 5637486.
Kelvin K. Ogilvie; Donald J. Iwacha. Use of the tert-butyldimethylsilyl group for protecting the hydroxyl functions of nucleosides. Tetrahedron Letters. 1973, s. 317–319. DOI 10.1016/S0040-4039(01)95650-3.
Leo A. Paquette; Iván Collado; Mark Purdie. Total Synthesis of Spinosyn A. 2. Degradation Studies Involving the Pure Factor and Its Complete Reconstitution. Journal of the American Chemical Society. 1998, s. 2553–2562. DOI 10.1021/ja974010k.

nih.gov

ncbi.nlm.nih.gov

Marc Lafrance; Keith Fagnou. Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design. Journal of the American Chemical Society. 2006-12-27, s. 16496–16497. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja067144j. PMID 17177387.
B. E. Griffin; M. Jarman; C. B. Reese. The Synthesis of oligoribonucleotides—IV. Tetrahedron. 1968, s. 639–662. DOI 10.1016/0040-4020(68)88015-9. PMID 5637486.

pubchem.ncbi.nlm.nih.gov

https://pubchem.ncbi.nlm.nih.gov/compound/6417

orgsyn.org

S. V. PUNTAMBEKER; E. A. ZOELLNER; L. T. SANDBORN; E. W. BOUSQUET. Trimethylacetic acid from tert.- Butyl Chloride. Org. Synth.. 1941. Dostupné online. DOI 10.15227/orgsyn.008.0104. ; Coll. Vol.. S. 524.
L. T. SANDBORN; E. W. BOUSQUET. Trimethylacetic acid from Pinacolone. Org. Synth.. 1941. Dostupné online. DOI 10.15227/orgsyn.008.0104. ; Coll. Vol.. S. 524.

web.archive.org

Dongbing Zhao; Weida Wang; Shuang Lian; Fei Yang; Jingbo Lan; Jingsong You. Phosphine-Free, Palladium-Catalyzed Arylation of Heterocycles through C−H Bond Activation with Pivalic Acid as a Cocatalyst. Chemistry – A European Journal. 2009-01-26, s. 16496–16497. Dostupné online. ISSN 0947-6539. DOI 10.1002/chem.200802001. Archivováno 31. 10. 2021 na Wayback Machine.

wiley.com

chemistry-europe.onlinelibrary.wiley.com

Dongbing Zhao; Weida Wang; Shuang Lian; Fei Yang; Jingbo Lan; Jingsong You. Phosphine-Free, Palladium-Catalyzed Arylation of Heterocycles through C−H Bond Activation with Pivalic Acid as a Cocatalyst. Chemistry – A European Journal. 2009-01-26, s. 16496–16497. Dostupné online. ISSN 0947-6539. DOI 10.1002/chem.200802001. Archivováno 31. 10. 2021 na Wayback Machine.

worldcat.org

Marc Lafrance; Keith Fagnou. Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design. Journal of the American Chemical Society. 2006-12-27, s. 16496–16497. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja067144j. PMID 17177387.
Dongbing Zhao; Weida Wang; Shuang Lian; Fei Yang; Jingbo Lan; Jingsong You. Phosphine-Free, Palladium-Catalyzed Arylation of Heterocycles through C−H Bond Activation with Pivalic Acid as a Cocatalyst. Chemistry – A European Journal. 2009-01-26, s. 16496–16497. Dostupné online. ISSN 0947-6539. DOI 10.1002/chem.200802001. Archivováno 31. 10. 2021 na Wayback Machine.