Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Aminopropanols"'
Publikováno v:
Russian Journal of General Chemistry. 89:2328-2332
The reactions of substituted 3-dietliylaminopropan-1-ones hydrochlorides with 2-amino-6-(H, alkyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carbonitriles and ethyl 2-amino-6-(H, methyl)-4,5,6,7-tetrariydrobenzo[b]-thiophene-3-carboxylate furnished β-am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96e400a9a03645f1d80b36f8de0763a8
https://doi.org/10.1134/s1070363219110264
https://doi.org/10.1134/s1070363219110264
Publikováno v:
Russian Journal of Organic Chemistry. 55:837-844
Six regioisomeric nonracemic dimethylphenyl glycerol ethers were synthesized by asymmetric dihydroxylation of the corresponding allyl dimethylphenyl ethers. The enantioselectivity of the reaction with o-methyl derivatives was lower (down to 34% ee) t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee378ddae002218af9d2e2c0ba65394b
https://doi.org/10.1134/s1070428019060149
https://doi.org/10.1134/s1070428019060149
Publikováno v:
Dhaka University Journal of Pharmaceutical Sciences. 15:235-239
not availableDhaka Univ. J. Pharm. Sci. 15(2): 235-239, 2016 (December)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7de06f9bab04e6423873023e26684505
https://doi.org/10.3329/dujps.v15i2.30943
https://doi.org/10.3329/dujps.v15i2.30943
Publikováno v:
Russian Journal of Organic Chemistry. 51:221-225
Reaction of N-methyl-6′,7′-dimethoxy-2′,3′-dihydro-1′H-spiro[cyclopentan-1,4′-isoquinoline]-1′-carboxamide with phenoxymethyloxiranes substituted in the aromatic ring afforded new propanediol derivatives, and from the epoxy derivative o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40a1b0a600c2ca845eb5a61a2b5e296f
https://doi.org/10.1134/s1070428015020153
https://doi.org/10.1134/s1070428015020153
Autor:
Zinaida Suvorova
Publikováno v:
ScienceRise: Biological Science; № 4 (7) (2017); 37-39
ScienceRise: Biological Science, Vol 0, Iss 4 (7), Pp 37-39 (2017)
ScienceRise: Biological Science, Vol 0, Iss 4 (7), Pp 37-39 (2017)
The aim of the research was to determine the therapeutic efficacy of the derivative of arilalifatic aminopropanols 1-[4-(1,1,3,3-tetramethyl butyl)phenoxi]-3-(N-benzyl hexamethylenimino)-2-propanol chloride (compound КВМ-194) in experiments in viv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::add44d3cd968883b0bcb8f994db1f09b
http://journals.uran.ua/sr_bio/article/view/109317
http://journals.uran.ua/sr_bio/article/view/109317
Publikováno v:
Applied Mechanics and Materials. 662:67-70
A series of α-aminophosphonate-functionalized 3-aminopropanols have been efficiently prepared and characterized by1H,13C, and31P NMR and mass spectroscopy. The reaction conditions such as solvent and temperature were thoroughly investigated based on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcb5847f79f66dcfa1a5f2d9d8e56d41
https://doi.org/10.4028/www.scientific.net/amm.662.67
https://doi.org/10.4028/www.scientific.net/amm.662.67
Autor:
Josef Jampilek, Jan Tengler, Ondřej Stropnický, Michal Oravec, Iva Kapustikova, Petr Mokrý, Jozef Csöllei
Publikováno v:
Open Chemistry, Vol 11, Iss 11, Pp 1757-1767 (2013)
Eight hydrochlorides of 3-{2-[(2/4-fluorophenoxy)-ethylamino]}-2-hydroxypropyl-4-alkoxybenzoates and four hydrochlorides of 3-tert-butylamino-2-hydroxypropyl-4-butoxybenzoates were prepared as potential antagonists of the β1-adrenergic receptor (bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d8549abdc8af1501b29781425f60d5
https://doaj.org/article/445cfe2af3944cb2a98fc364b117d4de
https://doaj.org/article/445cfe2af3944cb2a98fc364b117d4de
Autor:
A. G. Agababyan, G. A. Panosyan, A. E. Tumadzhyan, G. A. Gevorgyan, A. P. Avakyan, R. G. Paronikyan
Publikováno v:
Pharmaceutical Chemistry Journal. 47:361-365
Reduction of N-[β-(4-substituted benzoyl)ethyl]amino acids with sodium borohydride yielded arylaliphatic aminopropanols containing amino acid fragments – N-[3-(4-substituted phenyl)-3-hydroxypropyl]valines,-tryptophans, and 3-{[3-hydroxy-3-(4-subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b49f5ae78a09a978a8ba9455e2076ada
https://doi.org/10.1007/s11094-013-0959-5
https://doi.org/10.1007/s11094-013-0959-5
Autor:
A. U. Isakhanyan, S. G. Sharoyan, O. A. Papoyan, G. A. Gevorgyan, G. A. Panosyan, S. S. Mardanyan, I. G. Vermishyan
Publikováno v:
Pharmaceutical Chemistry Journal. 45:401-405
Aminomethylation of 4-substituted acetophenones yielded a series of β-amino-4-substituted propiophenones. Reduction of these with lithium alumohydride in dry ether produced 1-(4-substituted phenyl)-3-[4-substituted piperazino(piperidino)]propan-1-ol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97b132bc8933d9b653ec036876910fe4
https://doi.org/10.1007/s11094-011-0642-7
https://doi.org/10.1007/s11094-011-0642-7
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 186:945-951
The facile synthetic approaches to a wide range of potentially biologically active compounds bearing the cyclic 1,3,2-oxazaphosphinane moiety as a “cell transport” and the residues of formic, acetic, and amino acids or 3,5-bis(benzylidene)piperid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9fe5d39c020d2105b42f93cfb55c520
https://doi.org/10.1080/10426507.2010.520281
https://doi.org/10.1080/10426507.2010.520281