Relevant bibliographies by topics / Pyridinium dichromate

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Pyridinium dichromate'

Author: Grafiati
Published: 24 April 2022

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Journal articles on the topic "Pyridinium dichromate"

1

Liotta, Dennis, David Brown, William Hoekstra, and Robert Monahan. "Pyridinium dichromate-induced 1,3-oxidative rearrangements of enynols." Tetrahedron Letters 28, no. 10 (January 1987): 1069–72. http://dx.doi.org/10.1016/s0040-4039(00)95913-6.

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2

Czernecki, S., C. Georgoulis, C. L. Stevens, and K. Vijayakumaran. "Pyridinium dichromate oxidation. Modifications enhancing its synthetic utility." Tetrahedron Letters 26, no. 14 (January 1985): 1699–702. http://dx.doi.org/10.1016/s0040-4039(00)98314-x.

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Zhou, Jian, Yuefei Hu, and Hongwen Hu. "Synthesis of 5-(2-Phenylethenyl)indolizines by Selective Intermolecular 1,3-Dipolar Cycloaddition of 2-(2-Phenylethenyl)pyridinium N-Ylide with Alkenes Promoted by Tetrakis-pyridine Cobalt(II) Dichromate." Journal of Chemical Research 23, no. 2 (February 1999): 136–37. http://dx.doi.org/10.1177/174751989902300235.

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Intermolecular 1,3-dipolar cycloadditions of 2-(2-phenylethenyl)pyridinium N-ylides (3a–d) with electron-deficient alkenes (5a–d) were carried out selectively in the presence of tetrakis-pyridine cobalt(II) dichromate to yield 5-(2-phenylethenyl)indolizines (6a–j) in moderate yields (48–63%).
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Parish, Edward J., and Tsao-Yi Wei. "Allylic Oxidation of Δ5-Steroids with Pyridinium Chlorochromate (PCC) and Pyridinium Dichromate (PDC)." Synthetic Communications 17, no. 10 (July 1987): 1227–33. http://dx.doi.org/10.1080/00397918708063974.

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5

Dubberke, Silke, Muhammad Abbas, and Bernhard Westermann. "Oxidative allylic rearrangement of cycloalkenols: Formal total synthesis of enantiomerically pure trisporic acid B." Beilstein Journal of Organic Chemistry 7 (April 11, 2011): 421–25. http://dx.doi.org/10.3762/bjoc.7.54.

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Enantiomerically highly enriched unsaturated β-ketoesters bearing a quaternary stereocenter can be utilized as building blocks for the synthesis of natural occurring terpenes, i. a., trisporic acid and its derivatives. An advanced building block has been synthesized in a short reaction sequence, which involves an oxidative allylic rearrangement initiated by pyridinium dichromate (PDC) as the key step.
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Jordão, Alessandro. "Pyridinium Dichromate - A Mild Oxidizing Reagent in Synthetic Organic Chemistry." Synlett 2006, no. 19 (November 23, 2006): 3364–65. http://dx.doi.org/10.1055/s-2006-951561.

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7

KO, K. Y., and J. Y. PARK. "ChemInform Abstract: Aromatization of Hantzsch 1,4-Dihydropyridines with Pyridinium Dichromate." ChemInform 26, no. 46 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199546165.

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8

Meenakshisundaram, Subbiah, and M. Amutha. "Studies on the Oxidation of some Sulfides with Pyridinium Dichromate in Acetonitrile medium." Journal of Chemical Research 23, no. 1 (January 1999): 2–3. http://dx.doi.org/10.1177/174751989902300107.

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The kinetic behaviours of oxidation of dialkyl, alkyl aryl and diphenyl sulfides are quite different with pyridinium dichromate in acetonitrile medium; studies indicate the involvement of a sulfur cation free radical intermediate in diphenyl sulfide oxidation; electron releasing and withdrawing groups retard the reactivity of aryl methyl sulfides; the observed non-linear concave downwards type Hammett plot is well explained by assuming shifts in the rate-limiting step within the same overall reaction pathway.
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9

Kim, Jae Nyoung, and Eung K. Ryu. "Novel synthesis of lactonic nucleoside derivatives by pyridinium dichromate / acetic anhydride." Tetrahedron Letters 33, no. 22 (May 1992): 3141–44. http://dx.doi.org/10.1016/s0040-4039(00)79834-0.

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10

Richardson, R. T. "Formation of amorphous chromium dioxide by thermal decomposition of pyridinium dichromate." Journal of Materials Science Letters 8, no. 11 (November 1989): 1264–65. http://dx.doi.org/10.1007/bf00721487.

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Dissertations / Theses on the topic "Pyridinium dichromate"

1

ZHAN, YA-LING, and 詹雅玲. "Study of poly (vinyl pyridinium chlorochromate) and poly (vinyl pyridinium dichromate) as polymer reagents." Thesis, 1990. http://ndltd.ncl.edu.tw/handle/86749180499407585575.

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Book chapters on the topic "Pyridinium dichromate"

1

Yan, L., S. Lin, and P. Liu. "Using Pyridinium Dichromate." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00680.

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2

Figadère, B., and X. Franck. "With Pyridinium Dichromate." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00154.

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Parrain, J. L., and J. Thibonnet. "Using Pyridinium Dichromate or Pyridinium Chlorochromate." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00695.

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Lin, S., L. Yan, and P. Liu. "Oxidation Using Pyridinium Chlorochromate or Pyridinium Dichromate." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00075.

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Suffert, J. "Using Pyridinium Dichromate and Iodine." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00832.

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Lykakis, I. N., and M. Stratakis. "Allylic Peroxidation of Cycloalkenes with -Butyl Hydroperoxide Catalyzed by Pyridinium Chlorochromate or Pyridinium Dichromate." In Peroxides, Inorganic Esters (RO-X, X=Hal, S, Se, Te, N), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-038-00264.

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Lykakis, I. N., and M. Stratakis. "Reaction of Conjugated Dienes and Trienes with Pyridinium Dichromate and -Butyl Hydroperoxide." In Peroxides, Inorganic Esters (RO-X, X=Hal, S, Se, Te, N), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-038-00265.

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You might also be interested in the extended bibliographies on the topic 'Pyridinium dichromate' for particular source types:
Journal articles
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