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Mary Peters Fieser (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mary Peters Fieser" in Catalan language version.

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  • Pramer, Stacey «Mary Fieser: A transitional figure in the history of women». J. Chem. Educ., 62, 3, 1985, p. 186. DOI: 10.1021/ed062p186.
  • Fieser, Louis F.; Peters, Mary A. «The Potentials and the Decomposition Reactions of Ortho Qunones in Acid Solution». J. Am. Chem. Soc., 53, 2, 1931, p. 793–805. DOI: 10.1021/ja01353a053.. Fieser, Louis F.; Peters, Mary A. «The Addition of Diazomethane and some of its Derivatives to α-Naphthoquinone». J. Am. Chem. Soc., 53, 11, 1931, p. 4080–93. DOI: 10.1021/ja01362a024.. Fieser, Louis F.; Fieser, Mary «The Conversion of Phthaloylnaphthalenes and Naphthoyl-2-benzoic Acids into Benzanthraquinones». J. Am. Chem. Soc., 55, 8, 1933, p. 3342–52. DOI: 10.1021/ja01335a050.. Fieser, Louis F.; Fieser, Mary «The Tautomerism of the Aminonaphthoquinones». J. Am. Chem. Soc., 56, 7, 1934, p. 1565–78. DOI: 10.1021/ja01322a034.. Fieser, Louis F.; Fieser, Mary «The Reduction Potentials of Various Naphthoquinones». J. Am. Chem. Soc., 57, 3, 1935, p. 491–94. DOI: 10.1021/ja01306a031.. Fieser, Louis F.; Fieser, Mary «A New Diene Synthesis of Anthraquinones». J. Am. Chem. Soc., 57, 9, 1935, p. 1679–81. DOI: 10.1021/ja01312a054.. Fieser, Louis F.; Fieser, Mary «The Synthesis from β-Naphthohydroquinone of a Tautomer of 4-Benzyl-1,2-naphthoquinone». J. Am. Chem. Soc., 61, 3, 1939, p. 596–608. DOI: 10.1021/ja01872a017.. Fieser, Louis F.; Bowen, Douglas M.; Campbell, William P.; Fieser, Mary «Quinones having Vitamin K Activity». J. Am. Chem. Soc., 61, 7, 1939, p. 1925–26. DOI: 10.1021/ja01876a507.. Fieser, Mary; Fieser, Louis F. «Anthocyanidin-Like Pigments from α-Naphthohydroquinones». J. Am. Chem. Soc., 63, 6, 1941, p. 1572–76. DOI: 10.1021/ja01851a022.
  • Fieser, Louis F.; Fieser, Mary; Chakravarti, Ram Narayan «"α"-Spinasterol». J. Am. Chem. Soc., 71, 6, 1949, p. 2226–30. DOI: 10.1021/ja01174a085.. Fieser, Mary; Rosen, William E.; Fieser, Louis F. «An i-Steroid Hydrocarbon from Ergosterol». J. Am. Chem. Soc., 74, 21, 1952, p. 5397–5403. DOI: 10.1021/ja01141a052.. Fieser, Mary; Quilico, Adolfo; Nickon, Alex; Rosen, William E. «Permanganate Oxidation of Ergosterol». J. Am. Chem. Soc., 75, 16, 1953, p. 4066–71. DOI: 10.1021/ja01112a057.. Tarlton, E. James; Fieser, Mary; Fieser, Louis F. «Chromic Acid Oxidation of Epicholesteryl Acetate». J. Am. Chem. Soc., 75, 18, 1953, p. 4423–24. DOI: 10.1021/ja01114a007.. Fieser, Mary; Romero, Miguel A.; Fieser, Louis F. «Bromination of 5α,6β-Dibromocholestane-3-one». J. Am. Chem. Soc., 77, 12, 1955, p. 3305–7. DOI: 10.1021/ja01617a045.. Yamasaki, Kazumi; Rosnati, Vittorio; Fieser, Mary; Fieser, Louis F. «Δ3-Cholenic Acid». J. Am. Chem. Soc., 77, 12, 1955, p. 3308–9. DOI: 10.1021/ja01617a046.. Klass, Donald L.; Fieser, Mary; Fieser, Louis F. «Digitogenin». J. Am. Chem. Soc., 77, 14, 1955, p. 3829–33. DOI: 10.1021/ja01619a045.. Issidorides, Costas H.; Fieser, Mary; Fieser, Louis F. «Selenium Dioxide Oxidation of Methyl Δ3-Cholenate». J. Am. Chem. Soc., 82, 8, 1960, p. 2002–5. DOI: 10.1021/ja01493a038.
  • Fieser, Louis F.; Fieser, Mary «Naphthoquinone Antimalarials. XII. The Hooker Oxidation Reaction». J. Am. Chem. Soc., 70, 10, 1948, p. 3215–22. DOI: 10.1021/ja01190a005.
  • Bergman, Werner «New Books». J. Am. Chem. Soc., 66, 10, 1944, p. 1802. DOI: 10.1021/ja01238a056.. (book review)

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