Results 51 to 60 of about 97 (91)
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A Novel Method for the Stereoselective Synthesis of Tetralins and Indanes.
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Mike Casey +3 more
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Respiratory stimulating properties of some derivatives of indane
Toxicology and Applied Pharmacology, 1965Abstract An indane derivative of salicylic acid was found to stimulate respiration by reflex action through the carotid body. This action was greatly increased after depression with pentobarbital sodium, but not after cyclopropane. Evidence was presented of possible cardiovascular toxicity when large doses of the compound were administered ...
H W, NASH, D L, BOATMAN, J P, LONG
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Vanillin esters in reactions with indan-1,3-dione
Chemistry of Heterocyclic Compounds, 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
N. G. Kozlov, L. I. Basalaeva
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The Indans Formed by Dimerization of Some Aromatic Terpenoids
Australian Journal of Chemistry, 1986Previous work upon the dimerization of carvacrol derivatives to form indans is corrected.
Carman, Raymond M. +1 more
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Journal of Pharmaceutical Sciences, 1985
Aromatic hydroxylated derivatives of the spiro[indan-1,3'-pyrrolidine] and spiro[indan-2,2'-pyrrolidine] ring systems have been synthesized and evaluated for dopaminergic agonist and antagonist activities. None of these conformationally restricted catecholamines possessed any dopaminergic activity, but 5,6-dihydroxy spiro[indan-1,3'-pyrrolidine ...
R, Sommerville +2 more
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Aromatic hydroxylated derivatives of the spiro[indan-1,3'-pyrrolidine] and spiro[indan-2,2'-pyrrolidine] ring systems have been synthesized and evaluated for dopaminergic agonist and antagonist activities. None of these conformationally restricted catecholamines possessed any dopaminergic activity, but 5,6-dihydroxy spiro[indan-1,3'-pyrrolidine ...
R, Sommerville +2 more
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Canadian Journal of Chemistry, 1991
Indanes monosubstituted and 1,2- and 1,3-disubstituted in the pentagonal ring were synthesized, and configurations were assigned to the 1,2-disubstituted compounds by means of nuclear magnetic resonance spectroscopy. Key words: mono- and disubstituted indanes, conformation, configuration, 1H and 13C NMR, synthesis.
Elba N. Alesso +4 more
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Indanes monosubstituted and 1,2- and 1,3-disubstituted in the pentagonal ring were synthesized, and configurations were assigned to the 1,2-disubstituted compounds by means of nuclear magnetic resonance spectroscopy. Key words: mono- and disubstituted indanes, conformation, configuration, 1H and 13C NMR, synthesis.
Elba N. Alesso +4 more
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Method for the production of indanes.
1988Herstellung von Indanen durch Umsetzung von gegebenenfalls substituierten Benzylhalogeniden mit Olefinen in Gegenwart einer Lewis-Säure als Katalysator, indem man Benzylhalogenide I (mit R¹ und R² = Wasserstoff, Alkyl-, Alkoxy-, Cycloalkyl-, Aryl-, Aryloxy-, Aralkylrest R³ = R¹, Halogen oder ein ortho-kondensiertes Ringsystem X = Halogen) mit Olefinen
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Discovery of indane and naphthalene derivatives as USP7 inhibitors
European Journal of Medicinal ChemistryProtein deubiquitination via deubiquitinases is a crucial aspect of the dynamic modification of biomacromolecules. The deubiquitinase USP7 plays a key role in tumorigenesis through diverse pathways, thus representing a promising novel target for anti-cancer therapies. In this paper, in order to find novel USP7 inhibitors, a series of compounds scaffold-
Xian Zhang +18 more
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