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pro vyhledávání: '"James Cason"'
Autor:
James Cason
Publikováno v:
Organic Reactions
p-Benzoquinone or quinone was discovered in 1838 as a product of the action of manganese dioxide in sulfuric acid on the natural product, quinic acid, However, benzoquinones generally prepared by the oxidation of disubstituted aromatic hydrocarbons d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b48bf224258ad4f21b2f80aeae247b7
https://doi.org/10.1002/0471264180.or004.06
https://doi.org/10.1002/0471264180.or004.06
Autor:
James Cason
Publikováno v:
Organic Syntheses
β-Methylglutaric anhydride reactant: 115 g. (0.72 mole) of diethyl malonate reactant: 60 g. (0.60 mole) of methyl crotonate product: β-Methylglutaric anhydride product: methyl hydrogen β-methylglutarate Keywords: addition, to CC–CO and CC–CN;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::135cef4542ac133b4ac860c49158cb6f
https://doi.org/10.1002/0471264180.os038.20
https://doi.org/10.1002/0471264180.os038.20
Publikováno v:
Organic Syntheses
6-Ketohendecanedioic acid reactant: 89.3 g. (0.5 mole) of δ-carbomethoxyvaleryl chloride product: 6-ketohendecanedioic acid reactant: 100 g. (0.63 mole) of redistilled commercial methyl hydrogen adipate Keywords: elimination, dehydrohalogenation; hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c15c73b3c211c2c4d87e05d565e3c586
https://doi.org/10.1002/0471264180.os038.16
https://doi.org/10.1002/0471264180.os038.16
Publikováno v:
Organic Syntheses
Methyl hydrogen hendecanedioate intermediate: Dimethyl hendecanedioate product: Methyl hydrogen hendecanedioate Keywords: esterification, of dicarboxylic acids; hydrolysis, esters and lactones; barium hydroxide in methanol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49cdb9ee6642302ddfc3a968936acc57
https://doi.org/10.1002/0471264180.os038.21
https://doi.org/10.1002/0471264180.os038.21
Autor:
James Cason, Franklin S. Prout
Publikováno v:
Organic Syntheses
Methyl 4-keto-7-methyloctanoate reactant: 151 g. (1.0 mole) of pure isoamyl bromide product: methyl 4-keto-7-methyloctanoate reactant: methyl hydrogen succinate : Ethyl 10-keto-13-methyltetradecanoate : Ethyl 10-keto-16-methyloctadecanoate : Ethyl 6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3952e34f27226f145e783e1a8e8fe3fe
https://doi.org/10.1002/0471264180.os028.30
https://doi.org/10.1002/0471264180.os028.30
Autor:
James Cason
Publikováno v:
Organic Syntheses
β-Carbomethoxypropionyl chloride intermediate: Methyl hydrogen succinate reactant: 400 g. (4 moles) of succinic anhydride reactant: 290 ml. (4 moles) of thionyl chloride product: β-carbomethoxypropionyl chloride Keywords: acylation; replacement rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c908c1eda14b5c08fa2d3495a4cce755
https://doi.org/10.1002/0471264180.os025.07
https://doi.org/10.1002/0471264180.os025.07
Publikováno v:
The Journal of Organic Chemistry. 36:2621-2625