三氟过氧乙酸 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "三氟过氧乙酸" in Chinese language version.

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archive.org

Kürti, László; Czakó, Barbara. Strategic Applications of Named Reactions in Organic Synthesis. Elsevier Academic Press. 2005: 28. ISBN 9780124297852.
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Luxon, S. G. Hazards in the Chemical Laboratory 5th. Royal Society of Chemistry. 1992: 627. ISBN 9780851862293.
Cooper, Mark S.; Heaney, Harry; Newbold, Amanda J.; Sanderson, William R. Oxidation Reactions Using Urea–Hydrogen Peroxide; A Safe Alternative to Anhydrous Hydrogen Peroxide. Synlett. 1990, 1990 (9): 533–535. doi:10.1055/s-1990-21156.
Taylor, P. C. Vinyl and Aryl Chalcogenides: Sulfur-, Selenium- and Tellurium-based Functional Groups. Ley, Steven V. (编). Synthesis: Carbon with One Heteroatom Attached by a Single Bond. Comprehensive Organic Functional Group Transformations. Elsevier. 1995: 705–736. ISBN 9780080423234.
Page, P. C. B.; Wilkes, R. D.; Reynolds, D. Alkyl Chalcogenides: Sulfur-based Functional Groups. Ley, Steven V. (编). Synthesis: Carbon with One Heteroatom Attached by a Single Bond. Comprehensive Organic Functional Group Transformations. Elsevier. 1995: 113–276. ISBN 9780080423234.

archive.today

化工引擎. [2011-09-17]. （原始内容存档于2013-04-25）.

books.google.com

Hiyama, Tamejiro. 8.2 Trifluoroacetic acid and Trifluoroperacetic acid. Organofluorine Compounds: Chemistry and Applications. Springer Science & Business Media. 2000: 255–257 [2021-12-30]. ISBN 9783662041642. （原始内容存档于2021-12-30）.
Kataoka, T.; Yoshimatsu, M. Alkyl Chalcogenides: Selenium- and Tellurium-based Functional Groups. Ley, Steven V. (编). Synthesis: Carbon with One Heteroatom Attached by a Single Bond. Comprehensive Organic Functional Group Transformations. Elsevier. 1995: 277–296. ISBN 9780080423234.
Carey, Francis A.; Sundberg, Richard J. 5.5 Addition Reactions Involving Epoxides. Advanced Organic Chemistry: Part A: Structure and Mechanisms 5th. Springer Science & Business Media. 2007: 503–514 [2021-12-30]. ISBN 9780387448978. （原始内容存档于2021-12-30）.
Chambers, Richard D. Functional Compounds Containing Oxygen, Sulphur or Nitrogen and their Derivatives. Fluorine in Organic Chemistry. CRC Press. 2004: 242–243 [2021-12-30]. ISBN 9780849317903. （原始内容存档于2021-12-30）.
Carruthers, William. 6.3 Oxidation of Olefins. Some Modern Methods of Organic Synthesis. Cambridge University Press. 1971: 259–280 [2021-12-30]. ISBN 9780521096430. （原始内容存档于2021-12-30）.
Carruthers, William. 6.5 Baeyer–Villiger oxidation of ketones. Some Modern Methods of Organic Synthesis. Cambridge University Press. 1971: 287–290 [2021-12-30]. ISBN 9780521096430. （原始内容存档于2022-04-25）.
Hagen, Timothy J. Prilezhaev reaction. Li, Jie Jack; Corey, E. J. (编). Name Reactions of Functional Group Transformations. John Wiley & Sons. 2007: 274–281. ISBN 9780470176504.
Pirrung, Michael C.; Morehead, Andrew T.; Young, Bruce G. (编). 10. Neosporol, Sporol. Part B: Bicyclic and Tricyclic Sesquiterpenes. The Total Synthesis of Natural Products 11. John Wiley & Sons. 2000: 222–224 [2021-12-31]. ISBN 9780470129630. （原始内容存档于2022-05-05）.
Taylor, P. C. Vinyl and Aryl Chalcogenides: Sulfur-, Selenium- and Tellurium-based Functional Groups. Ley, Steven V. (编). Synthesis: Carbon with One Heteroatom Attached by a Single Bond. Comprehensive Organic Functional Group Transformations. Elsevier. 1995: 705–736. ISBN 9780080423234.
Page, P. C. B.; Wilkes, R. D.; Reynolds, D. Alkyl Chalcogenides: Sulfur-based Functional Groups. Ley, Steven V. (编). Synthesis: Carbon with One Heteroatom Attached by a Single Bond. Comprehensive Organic Functional Group Transformations. Elsevier. 1995: 113–276. ISBN 9780080423234.
Correia, Maria A.; Hollenberg, Paul F. Inhibition of Cytochrome P450 Enzymes. Ortiz de Montellano, Paul R. (编). Cytochrome P450: Structure, Mechanism, and Biochemistry 4th. Springer. 2015: 177–260 [2021-12-30]. ISBN 9783319121086. （原始内容存档于2022-04-12）.
Macherey, Anne-Christine; Dansette, Patrick M. Biotransformations Leading to Toxic Metabolites:Chemical Aspects. Wermuth, Camille Georges; Aldous, David; Raboisson, Pierre; Rognan, Didier (编). The Practice of Medicinal Chemistry 4th. Elsevier. 2015: 585–614 [2021-12-30]. ISBN 9780124172135. （原始内容存档于2021-12-30）.
Anslyn, Eric V.; Dougherty, Dennis A. 8.8 Miscellaneous Experiments for Studying Mechanism. Modern Physical Organic Chemistry. University Science Books. 2006: 471–482 [2021-12-30]. ISBN 9781891389313. （原始内容存档于2021-12-30）.

chemyq.com

化工引擎. [2011-09-17]. （原始内容存档于2013-04-25）.

doi.org

Caster, Kenneth C.; Rao, A. Somasekar; Mohan, H. Rama; McGrath, Nicholas A.; Brichacek, Matthew. Encyclopedia of Reagents for Organic Synthesis. e-EROS Encyclopedia of Reagents for Organic Synthesis. 2012. ISBN 978-0471936237. doi:10.1002/047084289X.rt254.pub2. |chapter=被忽略 (帮助)
Cooper, Mark S.; Heaney, Harry; Newbold, Amanda J.; Sanderson, William R. Oxidation Reactions Using Urea–Hydrogen Peroxide; A Safe Alternative to Anhydrous Hydrogen Peroxide. Synlett. 1990, 1990 (9): 533–535. doi:10.1055/s-1990-21156.
Ziegler, Fredrick E.; Metcalf, Chester A.; Nangia, Ashwini; Schulte, Gayle. Structure and total synthesis of sporol and neosporol. J. Am. Chem. Soc. 1993, 115 (7): 2581–2589. doi:10.1021/ja00060a006.
Emmons, William D.; FerrisEmmons, Arthur F. Oxidation Reactions with Pertrifluoroacetic Acid. J. Am. Chem. Soc. 1953, 75 (18): 4623–4624. doi:10.1021/ja01114a539.
Emmons, William D. Peroxytrifluoroacetic Acid. I. The Oxidation of Nitrosamines to Nitramines. J. Am. Chem. Soc. 1954, 76 (13): 3468–3470. doi:10.1021/ja01642a029.
Emmons, William D. Peroxytrifluoroacetic Acid. II. The Oxidation of Anilines to Nitrobenzenes. J. Am. Chem. Soc. 1954, 76 (13): 3470–3472. doi:10.1021/ja01642a030.
Emmons, William D.; Pagano, Angelo S.; Freeman, Jeremiah P. Peroxytrifluoroacetic Acid. III. The Hydroxylation of Olefins. J. Am. Chem. Soc. 1954, 76 (13): 3472–3474. doi:10.1021/ja01642a031.
Emmons, William D.; Pagano, Angelo S. Peroxytrifluoroacetic Acid. IV. The Epoxidation of Olefins. J. Am. Chem. Soc. 1955, 77 (1): 89–92. doi:10.1021/ja01606a029.
Emmons, William D.; Lucas, George B. Peroxytrifluoroacetic Acid. V. The Oxidation of Ketones to Esters. J. Am. Chem. Soc. 1955, 77 (8): 2287–2288. doi:10.1021/ja01613a077.
Emmons, William D.; Pagano, Angelo S. Peroxytrifluoroacetic Acid. VI. The Oxidation of Oximes to Nitroparaffins. J. Am. Chem. Soc. 1955, 77 (17): 4557–4559. doi:10.1021/ja01622a036.
Aubé, Jeffrey; Fehl, Charlie; Liu, Ruzhang; McLeod, Michael C.; Motiwala, Hashim F. 6.15 Hofmann, Curtius, Schmidt, Lossen, and Related Reactions. Heteroatom Manipulations. Comprehensive Organic Synthesis II 6. 1993: 598–635. ISBN 9780080977430. doi:10.1016/B978-0-08-097742-3.00623-6.
Prileschajew, Nikolaus. Oxydation ungesättigter Verbindungen mittels organischer Superoxyde [Oxidation of unsaturated compounds by means of organic superoxides]. Ber. Dtsch. Chem. Ges. 1909, 42 (4): 4811–4815 [2021-12-31]. doi:10.1002/cber.190904204100. （原始内容存档于2019-10-03）（德语）.
Hayakawa, Y.; Baba, Y.; Makino, S.; Noyori, R. Carbon-carbon bond formation promoted by transition metal carbonyls. 19. General synthesis of tropane alkaloids via the polybromo ketone-iron carbonyl reaction. J. Am. Chem. Soc. 1978, 100 (6): 1786–1791. doi:10.1021/ja00474a021.
Brooke, G. M.; Burdon, J.; Tatlow, J. C. Aromatic polyfluoro-compounds. Part VII. The reaction of pentafluoronitrobenzene with ammonia. J. Chem. Soc. 1961: 802–807. doi:10.1039/JR9610000802.
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Treiber, Alexander. Mechanism of the Aromatic Hydroxylation of Thiophene by Acid-Catalyzed Peracid Oxidation. J. Org. Chem. 2002, 67 (21): 7261–7266. PMID 12375952. doi:10.1021/jo0202177.
Mansuy, Daniel; Valadon, Philippe; Erdelmeier, Irene; López Garcia, Pilar; Amar, Claudine; Girault, Jean-Pierre; Dansette, Patrick M. Thiophene S-Oxides as new Reactive Metabolites: Formation by Cytochrome P-450 Dependent Oxidation and Reaction with Nucleophiles. J. Am. Chem. Soc. 1991, 113 (20): 7825–7826. doi:10.1021/ja00020a089.
Hart, Harold; Lerner, Lawrence R. Oxidations with peroxytrifluoroacetic acid-boron trifluoride. IX. Direct oxidation of alkenes to ketones using peroxytrifluoroacetic acid–boron fluoride. J. Org. Chem. 1967, 32 (9): 2669–2673. doi:10.1021/jo01284a004.
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Deno, Norman C.; Curry, Kenneth W.; Greigger, Barbara A.; Jones, A. Daniel; Rakitsky, Walter G.; Smith, Karen A.; Wagner, Karen; Minard, Robert D. Dihydroaromatic structure of Illinois No. 6 Monterey coal. Fuel. 1980, 59 (10): 694–698 [2021-12-31]. doi:10.1016/0016-2361(80)90021-6. （原始内容存档于2020-06-26）.
Chambers, R. D.; Cunningham, J. A.; Spring, D. J. Polyfluoroaryl organometallic compounds. Part VIII. Synthesis of and nucleophilic substitution in octafluorodibenzofuran. J. Chem. Soc. C. 1968: 1560–1565. doi:10.1039/J39680001560.
Berg, Ulf; Bladha, Håkan; Mpamposa, Konstantinos. Stereochemical variations on the colchicine motif. Peracid oxidation of thiocolchicone. Synthesis, conformation and inhibition of microtubule assembly. Org. Biomol. Chem. 2004, 2 (14): 2125–2130. PMID 15254641. doi:10.1039/B402840F.

harvard.edu

faculty.chemistry.harvard.edu

Myers, Andrew G. Chemistry 115 Handouts: Oxidation (PDF). Harvard University. [10 January 2017]. （原始内容 (PDF)存档于2017-05-16）.

kcsnet.or.kr

journal.kcsnet.or.kr

Kang, Ho-Jung; Jeong, Hee-Sun. New Method of Generating Trifluoroperoxyacetic acid for the Baeyer-Villiger Reaction. Bull. Korean Chem. Soc. 1996, 17 (1): 5–6 [2021-12-30]. （原始内容存档于2021-12-30）.

nih.gov

ncbi.nlm.nih.gov

Treiber, Alexander. Mechanism of the Aromatic Hydroxylation of Thiophene by Acid-Catalyzed Peracid Oxidation. J. Org. Chem. 2002, 67 (21): 7261–7266. PMID 12375952. doi:10.1021/jo0202177.
Berg, Ulf; Bladha, Håkan; Mpamposa, Konstantinos. Stereochemical variations on the colchicine motif. Peracid oxidation of thiocolchicone. Synthesis, conformation and inhibition of microtubule assembly. Org. Biomol. Chem. 2004, 2 (14): 2125–2130. PMID 15254641. doi:10.1039/B402840F.

orgsyn.org

Freeman, Jeremiah P. William D. Emmons: November 18, 1924 – December 8, 2001 (PDF). Org. Synth. November 14, 2002, 80: xxvii–xxix [January 21, 2017]. （原始内容 (PDF)存档于March 16, 2015）.
(1968) "2,3,4,5,6,6-Hexamethyl-2,4-cyclohexadien-1-one". Org. Synth. 48; Coll. Vol. 5: 598.
(1988) "Hofmann Rearrangement Under Mildly Acidic Conditions Using [I,I-Bis(Trifluoroacetoxy)Iodobenzene: Cyclobutylamine Hydrochloride from Cyclobutanecarboxamide]". Org. Synth. 66; Coll. Vol. 8: 132.

osti.gov

Deno, Norman C.; Curry, Kenneth W.; Greigger, Barbara A.; Jones, A. Daniel; Rakitsky, Walter G.; Smith, Karen A.; Wagner, Karen; Minard, Robert D. Dihydroaromatic structure of Illinois No. 6 Monterey coal. Fuel. 1980, 59 (10): 694–698 [2021-12-31]. doi:10.1016/0016-2361(80)90021-6. （原始内容存档于2020-06-26）.

web.archive.org

Hiyama, Tamejiro. 8.2 Trifluoroacetic acid and Trifluoroperacetic acid. Organofluorine Compounds: Chemistry and Applications. Springer Science & Business Media. 2000: 255–257 [2021-12-30]. ISBN 9783662041642. （原始内容存档于2021-12-30）.
Carey, Francis A.; Sundberg, Richard J. 5.5 Addition Reactions Involving Epoxides. Advanced Organic Chemistry: Part A: Structure and Mechanisms 5th. Springer Science & Business Media. 2007: 503–514 [2021-12-30]. ISBN 9780387448978. （原始内容存档于2021-12-30）.
Freeman, Jeremiah P. William D. Emmons: November 18, 1924 – December 8, 2001 (PDF). Org. Synth. November 14, 2002, 80: xxvii–xxix [January 21, 2017]. （原始内容 (PDF)存档于March 16, 2015）.
Chambers, Richard D. Functional Compounds Containing Oxygen, Sulphur or Nitrogen and their Derivatives. Fluorine in Organic Chemistry. CRC Press. 2004: 242–243 [2021-12-30]. ISBN 9780849317903. （原始内容存档于2021-12-30）.
Kang, Ho-Jung; Jeong, Hee-Sun. New Method of Generating Trifluoroperoxyacetic acid for the Baeyer-Villiger Reaction. Bull. Korean Chem. Soc. 1996, 17 (1): 5–6 [2021-12-30]. （原始内容存档于2021-12-30）.
Myers, Andrew G. Chemistry 115 Handouts: Oxidation (PDF). Harvard University. [10 January 2017]. （原始内容 (PDF)存档于2017-05-16）.
Carruthers, William. 6.3 Oxidation of Olefins. Some Modern Methods of Organic Synthesis. Cambridge University Press. 1971: 259–280 [2021-12-30]. ISBN 9780521096430. （原始内容存档于2021-12-30）.
Carruthers, William. 6.5 Baeyer–Villiger oxidation of ketones. Some Modern Methods of Organic Synthesis. Cambridge University Press. 1971: 287–290 [2021-12-30]. ISBN 9780521096430. （原始内容存档于2022-04-25）.
Prileschajew, Nikolaus. Oxydation ungesättigter Verbindungen mittels organischer Superoxyde [Oxidation of unsaturated compounds by means of organic superoxides]. Ber. Dtsch. Chem. Ges. 1909, 42 (4): 4811–4815 [2021-12-31]. doi:10.1002/cber.190904204100. （原始内容存档于2019-10-03）（德语）.
Pirrung, Michael C.; Morehead, Andrew T.; Young, Bruce G. (编). 10. Neosporol, Sporol. Part B: Bicyclic and Tricyclic Sesquiterpenes. The Total Synthesis of Natural Products 11. John Wiley & Sons. 2000: 222–224 [2021-12-31]. ISBN 9780470129630. （原始内容存档于2022-05-05）.
Correia, Maria A.; Hollenberg, Paul F. Inhibition of Cytochrome P450 Enzymes. Ortiz de Montellano, Paul R. (编). Cytochrome P450: Structure, Mechanism, and Biochemistry 4th. Springer. 2015: 177–260 [2021-12-30]. ISBN 9783319121086. （原始内容存档于2022-04-12）.
Macherey, Anne-Christine; Dansette, Patrick M. Biotransformations Leading to Toxic Metabolites:Chemical Aspects. Wermuth, Camille Georges; Aldous, David; Raboisson, Pierre; Rognan, Didier (编). The Practice of Medicinal Chemistry 4th. Elsevier. 2015: 585–614 [2021-12-30]. ISBN 9780124172135. （原始内容存档于2021-12-30）.
Anslyn, Eric V.; Dougherty, Dennis A. 8.8 Miscellaneous Experiments for Studying Mechanism. Modern Physical Organic Chemistry. University Science Books. 2006: 471–482 [2021-12-30]. ISBN 9781891389313. （原始内容存档于2021-12-30）.
Deno, Norman C.; Curry, Kenneth W.; Greigger, Barbara A.; Jones, A. Daniel; Rakitsky, Walter G.; Smith, Karen A.; Wagner, Karen; Minard, Robert D. Dihydroaromatic structure of Illinois No. 6 Monterey coal. Fuel. 1980, 59 (10): 694–698 [2021-12-31]. doi:10.1016/0016-2361(80)90021-6. （原始内容存档于2020-06-26）.

wikipedia.org

en.wikipedia.org

这种竞争具有生化意义。例如，环利尿剂替宁酸（英语：tienilic acid）是细胞色素P450的自杀型抑制剂，并且该抑制过程涉及噻吩的氧化。尽管有大量的研究，但是这个氧化途径仍不清楚。^[32]^[33]^[34]

zenodo.org

Prileschajew, Nikolaus. Oxydation ungesättigter Verbindungen mittels organischer Superoxyde [Oxidation of unsaturated compounds by means of organic superoxides]. Ber. Dtsch. Chem. Ges. 1909, 42 (4): 4811–4815 [2021-12-31]. doi:10.1002/cber.190904204100. （原始内容存档于2019-10-03）（德语）.