Zobrazeno 1 - 10 of 251 pro vyhledávání: '"Arthur C. Cope"'
2
The Alkylation of Esters and Nitriles
Autor: Herbert O. House, Arthur C. Cope, H. L Holmes
Publikováno v: Organic Reactions
This chapter is concerned with the reactions of metal salts (enolates) of active methylene compounds with alkylating agents such as alkyl halides to produce allyl derivatives. The first example of this reaction is found in the literature when Geuther
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6fa83c809fa678c58c198a36f36fbde3
https://doi.org/10.1002/0471264180.or009.04
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3
Methylenecyclohexane and N,N-Dimethylhydroxylamine Hydrochloride
Autor: Arthur C. Cope, Engelbert Ciganek
Publikováno v: Organic Syntheses
Methylenecyclohexane and N,N-dimethylhydroxylamine hydrochloride reactant: 49.4 g. (0.35 mole) of N,N-dimethylcyclohexylmethylamine product: methylenecyclohexane product: N,N-dimethylhydroxylamine hydrochloride Keywords: oxidation, R3N R3NO; thermal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d989e6867075190ab20c89cf2ec27921
https://doi.org/10.1002/0471264180.os039.14
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5
cis-Δ4-Tetrahydrophthalic Anhydride
Autor: Elbert C. Herrick, Arthur C. Cope
Publikováno v: Organic Syntheses
cis-Δ4-Tetrahydrophthalic anhydride reactant: 196 g. (2 moles) of maleic anhydride product: cis-Δ4-tetrahydrophthalic anhydride Keywords: addition, to CC–CC; annulation, carbocyclic-[6]; cyclization, cycloaddition; apparatus, for addition of buta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f26220932f610d9e75ae94a1a967cc90
https://doi.org/10.1002/0471264180.os030.34
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7
Cyclohexylidenecyanoacetic Acid and 1-Cyclohexenylacetonitrile
Autor: Donald Edward Whyte, Arthur C. Cope, Samuel A. Glickman, Alfred A. D'Addieco
Publikováno v: Organic Syntheses
Cyclohexylidenecyanoacetic acid and 1-cyclohexenylacetonitrile product: cyclohexylidenecyanoacetic acid product: 1-cyclohexenylacetonitrile Keywords: condensation, carbonyl-active methylene condensations; decarboxylation; separator, Dean and Stark
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::15e61076719375e06e65cab0cdacd246
https://doi.org/10.1002/0471264180.os031.09
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10
Ethyl (1-Ethylpropylidene)cyanoacetate
Autor: Evelyn M. Hancock, Arthur C. Cope
Publikováno v: Organic Syntheses
Ethyl (1-ethylpropylidene)cyanoacetate reactant: 67.8 g. (0.60 mole) of ethyl cyanoacetate reactant: 56.8 g. (0.66 mole) of diethyl ketone product: ethyl (1-ethylpropylidene)cyanoacetate Keywords: condensation, carbonyl-active methylene condensations
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7f9af709dd4f27283bc20ec6fd962a65
https://doi.org/10.1002/0471264180.os025.16
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