Zobrazeno 1 - 10
of 26
pro vyhledávání: '"E. Lukach"'
Publikováno v:
Bulgarian Journal of Veterinary Medicine, Vol 26, Iss 4, Pp 616-629 (2023)
The article is focused on microbiological safety of the traditional raw-dried meat product “Lukanka Panagyurska”, produced by a starter cultures, containing Lactiplantibacillus plantarum GLP3 and Debaryomyces hansenii ATCC 36239 instead of using
Externí odkaz:
https://doaj.org/article/bb8539a1358c46238e3d9cd73a0fc9d5
Publikováno v:
Oftalmologicheskii Zhurnal. 81:69-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ac920d0080378d7f6e8ed39dab03dbf
https://doi.org/10.31288/oftalmolzh201946974
https://doi.org/10.31288/oftalmolzh201946974
Akademický článek
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Autor:
Hua He, Ross D. Crosby, Paula Koeller, Megan E. Lukach, Janiece E. DeSocio, Julie K. O'Toole, Sarah A. Baird
Publikováno v:
European Eating Disorders Review. 20:e70-e77
Objective This study aimed to evaluate the psychometrics of the Rating of Eating Disorder Severity Interview for Children (REDS-C) and compare it with the Eating Disorder Inventory-2 symptom index. Methods The psychometrics of the REDS-C were analyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daf87e368477d6d42f5cbddc28c7aa01
https://doi.org/10.1002/erv.1115
https://doi.org/10.1002/erv.1115
Publikováno v:
The Journal of Organic Chemistry. 68:2807-2811
2-Substituted indoles (5a,b and 7) and fused indoles (9a-c, 11a,b, and 12) have been obtained by the S(RN)1 mechanism from photostimulated reactions of o-iodoaniline (1) and 1-halo-2-naphthalen-2-ylamines (3a,b) with enolate ions of acyclic (acetophe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171cdc5423f651e8e5d997e214c65f51
https://doi.org/10.1021/jo026672k
https://doi.org/10.1021/jo026672k
Publikováno v:
The Journal of Organic Chemistry. 66:5366-5373
Several bridgehead halobisnoradamantane derivatives (5, 7, 10, and 17) were synthesized from tricyclic diester 1 in good yields using standard methods. The reactivity through the SRN1 mechanism of the above compounds and the known halobisethano deriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e719a24d402e1eae8fd70114c2864db
https://doi.org/10.1021/jo010159+
https://doi.org/10.1021/jo010159+
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