Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Kimberly K. Larson"'
Autor:
Jennifer Lang, Brian B. Hasinoff, Kimberly K. Larson, Xing Wu, Jack C. Yalowich, Hong Liang, Lynn J. Guziec, Frank S. Jr. Guziec
Publikováno v:
Journal of Chemical Information and Modeling. 46:1827-1835
A series of 13 anthrapyrazole compounds that are analogues of piroxantrone and losoxantrone were synthesized, and their cell growth inhibitory effects, DNA binding, topoisomerase IIalpha mediated (EC 5.99.1.3) cleavage of DNA, and inhibition of DNA t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3931b756d218ab506d78f68ca6ab8afe
https://doi.org/10.1021/ci060056y
https://doi.org/10.1021/ci060056y
Publikováno v:
Imagination, Cognition and Personality. 16:51-61
Fifty volunteer participants were exposed to three experimental conditions. One group was given post-hypnotic suggestions urging them to remember certain types of material to be presented later. The second group was offered academic incentives throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48cf04491da898231a8bff6957ae2496
https://doi.org/10.2190/gkvq-lvy8-53fn-59e2
https://doi.org/10.2190/gkvq-lvy8-53fn-59e2
Autor:
Kimberly K. Larson, Richmond Sarpong
Publikováno v:
Journal of the American Chemical Society. 131(37)
Total synthesis of the Galbulimima alkaloid G. B. 13 was achieved utilizing a functionalized pyridine moiety as a piperidine surrogate. Key to the success of the synthesis was the development of an unprecedented rhodium-catalyzed 1,2-addition of an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c28873e6b41e0c081427bece070c163
https://pubmed.ncbi.nlm.nih.gov/19754185
https://pubmed.ncbi.nlm.nih.gov/19754185
Autor:
Hallie Taylor, Kimberly K. Larson, Xing Wu, Denny Lin, Brian B. Hasinoff, Jennifer Lang, Frank S. Guziec, Lynn J. Guziec, Paul Kerr, Asher Begleiter, Teresa Cabral
Publikováno v:
Oncology Reports.
Anthrapyrazoles have been investigated as cancer chemotherapeutic agents. The mechanism of action of these compounds is thought to involve inhibition of DNA topoisomerase II. A structure-activity study was carried out to determine the in vitro cytoto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c85d6bd110f9023d6b7427408e93b575
https://doi.org/10.3892/or.15.6.1575
https://doi.org/10.3892/or.15.6.1575
Autor:
Asher, Begleiter, Denny, Lin, Kimberly K, Larson, Jennifer, Lang, Xing, Wu, Teresa, Cabral, Hallie, Taylor, Lynn J, Guziec, Paul D, Kerr, Brian B, Hasinoff, Frank S, Guziec
Publikováno v:
Oncology reports. 15(6)
Anthrapyrazoles have been investigated as cancer chemotherapeutic agents. The mechanism of action of these compounds is thought to involve inhibition of DNA topoisomerase II. A structure-activity study was carried out to determine the in vitro cytoto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e361f7ee8a9f28d32b73b04f3c7b0a58
https://pubmed.ncbi.nlm.nih.gov/16685398
https://pubmed.ncbi.nlm.nih.gov/16685398
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f253deadb5064d98d050830548e5cd0
https://doi.org/10.1002/chin.200618065
https://doi.org/10.1002/chin.200618065
Autor:
Kees Goubitz, Kimberly K. Larson, Frank S. Jr. Guziec, Jan Fraanje, H. Schenk, Henk Hiemstra, J. Dijkink, Sanne Kuiper, Jan H. van Maarseveen, Bui T. B. Hue
Publikováno v:
Organic & Biomolecular Chemistry, 24, 4364-4366. Royal Society of Chemistry
The compact tricyclic substructure of solanoeclepin A containing the cyclobutanone ring was prepared by using as the key step a highly regioselective intramolecular [2 + 2]-photocycloaddition reaction between one of the π-bonds of an allene and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af92f5202d638d2febacd34d5f69701
https://doi.org/10.1002/chin.200420029
https://doi.org/10.1002/chin.200420029
Autor:
Bui T B, Hue, Jan, Dijkink, Sanne, Kuiper, Kimberly K, Larson, Frank S, Guziec, Kees, Goubitz, Jan, Fraanje, Henk, Schenk, Jan H, van Maarseveen, Henk, Hiemstra
Publikováno v:
Organicbiomolecular chemistry. 1(24)
The compact tricyclic substructure of solanoeclepin A containing the cyclobutanone ring was prepared by using as the key step a highly regioselective intramolecular [2 + 2]-photocycloaddition reaction between one of the [small pi]-bonds of an allene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c4c26969375b6f3c5c579fa91492ec4
https://pubmed.ncbi.nlm.nih.gov/14685306
https://pubmed.ncbi.nlm.nih.gov/14685306
Publikováno v:
Chemical Science. 3:1825
A shapeshifting organic molecule dynamically adjusts its equilibrium population of discrete structural isomers in response to an analyte. By incorporating a single 13C-label into the bullvalene core, these changes can be read by a single 13C NMR expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dbad9d058f5cccfae1df2910277bf9c
https://doi.org/10.1039/c2sc20238g
https://doi.org/10.1039/c2sc20238g
Autor:
Jan H. van Maarseveen, Kimberly K. Larson, Henk Hiemstra, H. Schenk, Kees Goubitz, J. Dijkink, Sanne Kuiper, Bui T. B. Hue, Jan Fraanje, Frank S. Jr. Guziec
Publikováno v:
Organic & Biomolecular Chemistry. 1:4364
The compact tricyclic substructure of solanoeclepin A containing the cyclobutanone ring was prepared by using as the key step a highly regioselective intramolecular [2 + 2]-photocycloaddition reaction between one of the π-bonds of an allene and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::842342e49671eb6c2ac70895c8bf30cf
https://doi.org/10.1039/b311415e
https://doi.org/10.1039/b311415e