Zobrazeno 1 - 10 of 10 pro vyhledávání: '"M. A. Eissenstat"'
1
(Aminoalkyl)indole Isothiocyanates as Potential Electrophilic Affinity Ligands for the Brain Cannabinoid Receptor
Autor: J. L. Flippen-Anderson, Allyn C. Howlett, Koichiro Yamada, Susan Jean Ward, M. A. Eissenstat, Kenner C. Rice, Johnson Mr
Publikováno v: Journal of Medicinal Chemistry. 39:1967-1974
A series of (aminoalkyl)indole compounds, naphthalene analogs of pravadoline (1), has been shown to exhibit cannabinoid agonist activities such as antinociception in animals, inhibition of adenylate cyclase in brain membranes, and binding to the cann
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::650fc55168b4a1dadd1333447d64d11a
https://doi.org/10.1021/jm950932r
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2
Transfer of activation from indoles to alcohols: A new method for the synthesis of aminoethylindoles
Autor: M. A. Eissenstat, John D. Weaver
Publikováno v: Tetrahedron Letters. 36:2029-2032
Transfer of a sulfonyl group from an indole nitrogen to a β-amino alkoxide generates an indole anion and an aminoethylsulfonate which react to give aminoethylindoles.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::155eb0601b8ae1f6ac03ce5ce5b136b2
https://doi.org/10.1016/0040-4039(95)00229-6
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3
A retro-Diels-Alder approach to oxazoles and imidazoles
Autor: M. A. Eissenstat, John D. Weaver
Publikováno v: The Journal of Organic Chemistry. 58:3387-3390
Heating N-acyl derivatives 4 of 3-endo-aminobicyclo[2.2.1]hept-5-en-2-endo-ol (3) at 185-195 o C 4-5 h provides oxazoles 1a-e in 49-88% yields. The reaction proceeds via initial dehydration to an oxazoline which undergoes retro-Diels-Alder reaction t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::18980586c64b768f066b5c261089c4aa
https://doi.org/10.1021/jo00064a029
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4
ChemInform Abstract: Transfer of Activation from Indoles to Alcohols: A New Method for the Synthesis of Aminoethylindoles
Autor: John D. Weaver, M. A. Eissenstat
Publikováno v: ChemInform. 26
Transfer of a sulfonyl group from an indole nitrogen to a β-amino alkoxide generates an indole anion and an aminoethylsulfonate which react to give aminoethylindoles.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8c494c47d0a3175ca90ebc6a91df32df
https://doi.org/10.1002/chin.199530132
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6
ChemInform Abstract: (Aminoalkyl)indole Isothiocyanates as Potential Electrophilic Affinity Ligands for the Brain Cannabinoid Receptor
Autor: Allyn C. Howlett, Johnson Mr, M. A. Eissenstat, J. L. Flippen-Anderson, Kenner C. Rice, Koichiro Yamada, Susan Jean Ward
Publikováno v: ChemInform. 27
A series of (aminoalkyl)indole compounds, naphthalene analogs of pravadoline (1), has been shown to exhibit cannabinoid agonist activities such as antinociception in animals, inhibition of adenylate cyclase in brain membranes, and binding to the cann
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d6185d922494e1a695cb63785370b188
https://doi.org/10.1002/chin.199635118
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8
Nitriles from Ketones: Cyclohexanecarbonitrile
Autor: N. Sapuppo, Paul A. Wender, M. A. Eissenstat, Frederick E. Ziegler
Publikováno v: Organic Syntheses
Nitriles from ketones: cyclohexanecarbonitrile intermediate: Methyl 2-(1-cyanocyclohexyl)hydrazine carboxylate (1) intermediate: Methyl 2-(1-cyancyclohexyl)diaxenecarboxylate (2) product: cyclohexanecarbonitrile (3) Keywords: condensation, miscellane
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::573091d02dc180a7aab2646ee545f418
https://doi.org/10.1002/0471264180.os058.18
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