Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Frank, Moffatt"'
Publikováno v:
CHIMIA, Vol 63, Iss 12 (2009)
Externí odkaz:
https://doaj.org/article/abae99e368694fb2be011aa75e522c80
Publikováno v:
CHIMIA, Vol 63, Iss 6 (2009)
Externí odkaz:
https://doaj.org/article/bfc3755ef5224f00baa67079ebc9763c
Autor:
Oscar, Salas-Solano, Babu, Kennel, SungAe Suhr, Park, Kelly, Roby, Zoran, Sosic, Boris, Boumajny, Sarah, Free, Angelia, Reed-Bogan, David, Michels, Will, McElroy, Pauline, Bonasia, Mingfang, Hong, Xiaoping, He, Margaret, Ruesch, Frank, Moffatt, Steffen, Kiessig, Brian, Nunnally
Publikováno v:
Journal of separation science. 35(22)
An international team including 12 laboratories from 11 independent biopharmaceutical companies in the United States and Switzerland was formed to evaluate the precision and robustness of imaged capillary isoelectric focusing for the charge heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc4d4a4e50b7d62d0944adf80529fddb
https://pubmed.ncbi.nlm.nih.gov/23065998
https://pubmed.ncbi.nlm.nih.gov/23065998
Publikováno v:
CHIMIA. 63:885
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::202b9ac33d076f55ae743abee659fada
https://doi.org/10.2533/chimia.2009.885
https://doi.org/10.2533/chimia.2009.885
Publikováno v:
CHIMIA. 63:350
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa8c2f4c6ac298523e6e9d7b6cd0690e
https://doi.org/10.2533/chimia.2009.350
https://doi.org/10.2533/chimia.2009.350
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3143
The 2-hydroxyisopropyl (1 -hydroxy-1 -methylethyl) segment derived from a prenyl residue occurs in a number of natural products, including the rotenoid dalpanol, and the aim of this work is the identification and isotopic labelling of the (pro-R) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d099f88b1900ad5615ea573d6d14ff9
https://doi.org/10.1039/p19910003143
https://doi.org/10.1039/p19910003143
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :779-788
Treated with boron tribromide (–)-(6aS,12aS,5′R)-rotenone is converted first into a primary allylic bromide by ring-E cleavage, then into the 2-de-O-methyl and finally the 2,3-dide-O-methyl derivatives. With (6aS,12aS,5′R)-6′7′-dihydroroten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6dbaa1dbf8879488a94b1f4294ce18
https://doi.org/10.1039/p19820000779
https://doi.org/10.1039/p19820000779