Norrishova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Norrishova reakce" in Czech language version.

refsWebsite

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10doi.org

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3iupac.org

538^th place

244^th place

2harvard.edu

18^th place

99^th place

1orgsynth.org

low place

5,380^th place

1nih.gov

4^th place

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doi.org

Guido Grause; Mei-Fang Chien; Chihiro Inoue. Changes during the weathering of polyolefins. Polymer Degradation and Stability. 2020, s. 109364. doi:10.1016/j.polymdegradstab.2020.109364.
IUPAC Gold Book - Norrish Type I photoreaction. [s.l.]: IUPAC, 2014-03-31. Dostupné online. doi:10.1351/goldbook.N04219.
Nien-Chu Yang; Eugene D. Feit; Man Him Hui; Nicholas J. Turro; Christopher Dalton. Photochemistry of di-tert-butyl ketone and structural effects on the rate and efficiency of intersystem crossing of aliphatic ketones. Journal of the American Chemical Society. 1970, s. 6974–6976. doi:10.1021/ja00726a046.
E. B. Abuin; M. V. Encina; E. A. Lissi. The photolysis of 3-pentanone. Journal of Photochemistry. 1972, s. 387–396. doi:10.1016/0047-2670(72)80036-4.
IUPAC Gold Book - Norrish Type II photoreaction. [s.l.]: IUPAC, 2014-02-24. Dostupné online. doi:10.1351/goldbook.N04218.
R. G. W. Norrish; C. H. Bamford. Photo-decomposition of Aldehydes and Ketones. Nature. 1937-07-31, s. 195–196. doi:10.1038/140195b0. Bibcode 1937Natur.140..195N.
IUPAC Gold Book - Norrish–Yang reaction. [s.l.]: IUPAC, 2014-03-31. Dostupné online. doi:10.1351/goldbook.NT07427.
Photolysis of Heptanal Suzanne E. Paulson, De-Ling Liu, Grazyna E. Orzechowska, Luis M. Campos, and K. N. Houk The Journal of Organic Chemistry; 2006; 71(17) pp 6403 - 6408; doi:10.1021/jo060596u
Facile Photochemical Synthesis of Unprotected Aqueous Gold Nanoparticles Katherine L. McGilvray, Matthew R. Decan, Dashan Wang, and Juan C. Scaiano Journal of the American Chemical Society; 2006; 128(50) pp 15980 - 15981; doi:10.1021/ja066522h
H. Renata; Q. Zhou; P. S. Baran. Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide. Science. 2013-01-03, s. 59–63. doi:10.1126/science.1230631. PMID 23288535. Bibcode 2013Sci...339...59R.

harvard.edu

adsabs.harvard.edu

R. G. W. Norrish; C. H. Bamford. Photo-decomposition of Aldehydes and Ketones. Nature. 1937-07-31, s. 195–196. doi:10.1038/140195b0. Bibcode 1937Natur.140..195N.
H. Renata; Q. Zhou; P. S. Baran. Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide. Science. 2013-01-03, s. 59–63. doi:10.1126/science.1230631. PMID 23288535. Bibcode 2013Sci...339...59R.

iupac.org

goldbook.iupac.org

IUPAC Gold Book - Norrish Type I photoreaction. [s.l.]: IUPAC, 2014-03-31. Dostupné online. doi:10.1351/goldbook.N04219.
IUPAC Gold Book - Norrish Type II photoreaction. [s.l.]: IUPAC, 2014-02-24. Dostupné online. doi:10.1351/goldbook.N04218.
IUPAC Gold Book - Norrish–Yang reaction. [s.l.]: IUPAC, 2014-03-31. Dostupné online. doi:10.1351/goldbook.NT07427.

nih.gov

ncbi.nlm.nih.gov

H. Renata; Q. Zhou; P. S. Baran. Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide. Science. 2013-01-03, s. 59–63. doi:10.1126/science.1230631. PMID 23288535. Bibcode 2013Sci...339...59R.

orgsynth.org

Bicyclohexylidene Nicholas J. Turro, Peter A. Leermakers, George F. Vesley Organic Syntheses, Coll. Vol. 5, p. 297 (1973); Vol. 47, p. 34 (1967) Online.