Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Paulina Rogowska"'
Publikováno v:
Studia Medyczne, Vol 39, Iss 4, Pp 364-375 (2023)
Externí odkaz:
https://doaj.org/article/3f9fa8ea404d40b0b2efc961599aca08
Publikováno v:
Tetrahedron Letters. 47:1389-1393
Strong heterodimeric interactions of phenylboronic acids with l -proline or betaine are evident in the solid state. The interaction energy is over 23 kcal/mol (at MP2/6-31+G∗).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ceef70416b53317e8ee70d3f58b7d1b
https://doi.org/10.1016/j.tetlet.2005.12.105
https://doi.org/10.1016/j.tetlet.2005.12.105
Publikováno v:
Carbohydrate Research. 340:2645-2653
The X-ray diffraction analysis of N-p-nitrophenyl-α- d -ribopyranosylamine (1) and N-p-nitrophenyl-α- d -xylopyranosylamine (2) was performed. It was found that an independent part of the unit cell of compound 1 is formed by three molecules of suga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0a8e7e48f3ccd9c62bb21293778c0a2
https://doi.org/10.1016/j.carres.2005.09.009
https://doi.org/10.1016/j.carres.2005.09.009
Publikováno v:
Carbohydrate Research. 340:1175-1184
The X-ray diffraction analysis of o-nitrophenyl 2,3,4,6-tetra-O-acetyl-β- d -galactopyranoside (1), m-nitrophenyl 2,3,4,6-tetra-O-acetyl-β- d -galactopyranoside, p-nitrophenyl 2,3,4,6-tetra-O-acetyl-β- d -galactopyranoside and o-nitrophenyl 2,3,4,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8fe84498e8531959e3f2b45a2521017
https://doi.org/10.1016/j.carres.2005.02.010
https://doi.org/10.1016/j.carres.2005.02.010
Autor:
Andrzej, Temeriusz, Tomasz, Gubica, Paulina, Rogowska, Katarzyna, Paradowska, Michał K, Cyrański
Publikováno v:
Carbohydrate research. 340(17)
The X-ray diffraction analysis of N-p-nitrophenyl-alpha-D-ribopyranosylamine (1) and N-p-nitrophenyl-alpha-D-xylopyranosylamine (2) was performed. It was found that an independent part of the unit cell of compound 1 is formed by three molecules of su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::121920641eac118b9f1658f716d4fa95
https://pubmed.ncbi.nlm.nih.gov/16199023
https://pubmed.ncbi.nlm.nih.gov/16199023
Publikováno v:
Applied Organometallic Chemistry. 19:1202-1203
o-Formylphenylboronic acid reacts with morpholine to form 1,3-dihydro-1-hydroxy-3-morpholin-4-yl-2,1-benzoxaborole. The typical hydrogen-bonded dimer motif with a planar benzoxaborole fragment has been obtained in the solid state. Copyright © 2005 J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::261b5a7da7f855b27f75508ee79ca3fc
https://doi.org/10.1002/aoc.991
https://doi.org/10.1002/aoc.991