Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Milosz Grabski"'
Autor:
Ting Qin, Milosz Grabski, Daniel Fitzpatrick, James Salsbury, Tracey Allford, Jeremy Pole, Andrew Novak, Jason Shiers, Colin Sambrook Smith
Publikováno v:
SLAS Technology, Vol 27, Iss 3, Pp 204-208 (2022)
Within a growing drug discovery company, hundreds of scientists take and move reagent chemicals on a daily basis. Conveniently updating the locations of tens of thousands of chemical containers in an electronic system is a big challenge. We have an e
Externí odkaz:
https://doaj.org/article/ffd65eb5ea744d5c9812e337fb392454
Publikováno v:
Organic Letters. 15:370-373
A new method for ketone enolate C-acylation is described which utilizes alkyl pentafluorophenylcarbonates, thiocarbonates, and thionocarbonates as the reactive acylating agents, and MgBr(2)·Et(2)O, DMAP, and i-Pr(2)NEt as the reagents for enolizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d86a498aa92c6f30cda18bff06dd59
https://doi.org/10.1021/ol303324a
https://doi.org/10.1021/ol303324a
Publikováno v:
Veterinary surgery : VS. 45(4)
To describe the volume and dimensions of the bicipital bursa and its position in relation to bony and soft tissue structures, in order to develop a novel medial synoviocentesis approach to the bicipital bursa.Cadaveric study.Adult equine cadaver limb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aea4f103efdaaab74f126b8550dcef5d
https://pubmed.ncbi.nlm.nih.gov/27062252
https://pubmed.ncbi.nlm.nih.gov/27062252
Autor:
Karl J. Hale, Soraya Manaviazar, Milosz Grabski, Jun Ishihara, Maciej Maczka, Susumi Hatakeyama, Fumiya Urabe
Publikováno v:
ChemInform. 46
Stereochemical evidence is presented to demonstrate that (−)-inthomycin C has (3R)- and not (3S)-stereochemistry. Careful reappraisal of the previously published work2−5 now indicates that the Hata...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6792571505a4c3b74a60c67322e6d7df
https://doi.org/10.1002/chin.201502196
https://doi.org/10.1002/chin.201502196
Publikováno v:
ChemInform. 45
A new pathway to (+)-inthomycin C is reported that exploits an O-directed free radical hydrostannation reaction on (−)-12 and a Stille cross-coupling as key steps. Significantly, the latter process was effected on 19 where a gauche-pentane repulsiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fde7eb6f4b6da2042c567970263ae9b3
https://doi.org/10.1002/chin.201431217
https://doi.org/10.1002/chin.201431217
Autor:
Soraya Manaviazar, Fumiya Urabe, Jun Ishihara, Susumi Hatakeyama, Milosz Grabski, Maciej Maczka, Karl J. Hale
Publikováno v:
Organic letters. 16(13)
Stereochemical evidence is presented to demonstrate that (-)-inthomycin C has (3R)- and not (3S)-stereochemistry. Careful reappraisal of the previously published work2-5 now indicates that the Hatakeyama, Hale, Ryu, and Taylor teams all have synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c47f79098c8c029881159da9cead83
https://pubmed.ncbi.nlm.nih.gov/24957611
https://pubmed.ncbi.nlm.nih.gov/24957611
Publikováno v:
Organic letters. 16(4)
A new pathway to (+)-inthomycin C is reported that exploits an O-directed free radical hydrostannation reaction on (−)-12 and a Stille cross-coupling as key steps. Significantly, the latter process was effected on 19 where a gauche-pentane repulsiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1962ebacb480f0f41edf81affcf2d2c
https://pubmed.ncbi.nlm.nih.gov/24502463
https://pubmed.ncbi.nlm.nih.gov/24502463
Autor:
Amarjit Kaur, Mehrnoosh Ostovar, Maciej Maczka, Milosz Grabski, Karl J. Hale, Soraya Manaviazar
Publikováno v:
Organic letters. 16(4)
Herein a new double O-directed free radical hydrostannation reaction is reported on the structurally complex dialkyldiyne 11. Through our use of a conformation-restraining acetal to help prevent stereocenter-compromising 1,5-H-atom abstraction reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461fe7dbb9315af5d9793d8bb296323b
https://pubmed.ncbi.nlm.nih.gov/24502452
https://pubmed.ncbi.nlm.nih.gov/24502452
Publikováno v:
ChemInform. 44
A new method for ketone enolate C-acylation is described which utilizes alkyl pentafluorophenylcarbonates, -thiocarbonates, and -thionocarbonates as reactive acylating agents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b255c3b234780ba71b9f688134786066
https://doi.org/10.1002/chin.201324035
https://doi.org/10.1002/chin.201324035