Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Andres E. Lukach"'
Publikováno v:
Molecules, Vol 29, Iss 13, p 3011 (2024)
Solifenacin (SFC) is a potent muscarinic antagonist that effectively reduces bladder muscle contraction, thereby alleviating symptoms such as frequency of micturition and urgency. Oxidation of SFC leads to the formation of impurities like Impurity K.
Externí odkaz:
https://doaj.org/article/42af68b57e0443c49359fdeb4f812e1d
Publikováno v:
Tetrahedron. 57:2419-2425
The strain of the bisnoradamantane skeleton is shown by: (i) the easy homoketonization of tricyclo[3.3.0.0 3,7 ]octane-1,5-diol, 2a , to exo -7-hydroxy- cis -bicyclo[3.3.0]octan-3-one, 3a , under silica gel column chromatography, and (ii) the cleavag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6caef6ab5c03fed40e7bfdc62ff28da9
https://doi.org/10.1016/s0040-4020(01)00096-5
https://doi.org/10.1016/s0040-4020(01)00096-5
Publikováno v:
Tetrahedron. 56:2703-2707
Carboxylic acids are bromodecarboxylated in moderate to good yields on reaction with iodosobenzene diacetate and bromine under irradiation with a tungsten lamp. The reaction works very well with carboxylic acids having a primary, secondary or tertiar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a565f69b966cdea73da22354147b4fb7
https://doi.org/10.1016/s0040-4020(00)00169-1
https://doi.org/10.1016/s0040-4020(00)00169-1
Autor:
Roberto A. Rossi, Andres E. Lukach
Publikováno v:
The Journal of Organic Chemistry. 64:5826-5831
The reaction of 2-iodoadamantane (1) with the potassium enolate of acetophenone (2) did not occur in the dark but succeeded under irradiation or in the presence of FeBr2 to give the substitution product 3 in 62% and 88% yields, respectively. The phot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a585f94f8583b73ea138ce71294a0f0c
https://doi.org/10.1021/jo990156l
https://doi.org/10.1021/jo990156l
Publikováno v:
The Journal of Organic Chemistry. 62:4260-4265
The reactions of 1,3-dihaloadamantanes with various carbanionic nucleophiles were studied. Potassium enolates of acetophenone (2) and pinacolone (10b) and the anion of nitromethane (10a) reacted with 1,3-diiodoadamantane (1a) in DMSO under photostimu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14914017c2361d41f250a04d102fea95
https://doi.org/10.1021/jo9620728
https://doi.org/10.1021/jo9620728
Publikováno v:
The Journal of Organic Chemistry. 60:1000-1004
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78b7ee2d9998615449bcb4e5e5f02554
https://doi.org/10.1021/jo00109a035
https://doi.org/10.1021/jo00109a035
Publikováno v:
Journal of Physical Organic Chemistry. 7:610-614
The reactivity of 1,3-dihaloadamantanes with diphenylphosphide ions (Ph2P−) in liquid ammonia was studied. 1,3-Dichloroadamantane (1a), 1-bromo-3-chloroadamantane (1b) and 1,3-dibromoadamantane (1c) reacted with Ph2P− ions under photostimulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f528b1837f0188e58d0deb52646f040
https://doi.org/10.1002/poc.610071104
https://doi.org/10.1002/poc.610071104
Autor:
Roberto A. Rossi, Andres E. Lukach
Publikováno v:
ChemInform. 30
The reaction of 2-iodoadamantane (1) with the potassium enolate of acetophenone (2) did not occur in the dark but succeeded under irradiation or in the presence of FeBr2 to give the substitution product 3 in 62% and 88% yields, respectively. The phot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::016474dcc6ad477f305e698bdae11aaf
https://doi.org/10.1002/chin.199946085
https://doi.org/10.1002/chin.199946085
Publikováno v:
ChemInform. 31
Carboxylic acids are bromodecarboxylated in moderate to good yields on reaction with iodosobenzene diacetate and bromine under irradiation with a tungsten lamp. The reaction works very well with carboxylic acids having a primary, secondary or tertiar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6de6db29f150e333b45dfee7df143c72
https://doi.org/10.1002/chin.200031070
https://doi.org/10.1002/chin.200031070
Publikováno v:
ChemInform. 32
The strain of the bisnoradamantane skeleton is shown by: (i) the easy homoketonization of tricyclo[3.3.0.0 3,7 ]octane-1,5-diol, 2a , to exo -7-hydroxy- cis -bicyclo[3.3.0]octan-3-one, 3a , under silica gel column chromatography, and (ii) the cleavag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de51436608e78414fa4bad3fb64a1e5c
https://doi.org/10.1002/chin.200129089
https://doi.org/10.1002/chin.200129089