Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kevin P. Lund"'
Autor:
Heather C Mefford, Peiwen Zhou, Cynthia Friedman, Melanie P. Gygi, Mark L. Stolowitz, Mark D. Ferguson, Kevin P. Lund, Barbara J. Trask, Ger van den Engh, Christine L. O'Day
Publikováno v:
Nucleic Acids Research. 30:2790-2799
In this paper, we demonstrate the use of synthetic polyamide probes to fluorescently label heterochromatic regions on human chromosomes for discrimination in cytogenetic preparations and by flow cytometry. Polyamides bind to the minor groove of DNA i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6239ad2d56493fe1a1b26f61935cd35
https://doi.org/10.1093/nar/gkf406
https://doi.org/10.1093/nar/gkf406
Autor:
Mark L. Stolowitz, Clarence N. Ahlem, Jean P. Wiley, Guisheng Li, Robert J. Kaiser, Karin A. Hughes, Edward A. Kesicki, Torkelson Steven M, Kevin P. Lund
Publikováno v:
Bioconjugate Chemistry. 12:229-239
A chemical affinity system exhibiting antibody-like properties is described. The system exploits bioconjugates with appended phenylboronic acid (PBA) moieties and a support-bound phenylboronic acid complexing reagent derived from salicylhydroxamic ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558b8cc0b7c2fe0e707f295a72edd9ea
https://doi.org/10.1021/bc0000942
https://doi.org/10.1021/bc0000942
Autor:
Kevin P. Lund, Daniel F. Harvey
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95cde7be758c0e93c1fd72783549de92
https://doi.org/10.1002/chin.199209137
https://doi.org/10.1002/chin.199209137
ChemInform Abstract: Cyclization Reactions of a Molybdenum Carbene Complex with 1,3- Nonadien-8-ynes
Autor:
Daniel F. Harvey, Kevin P. Lund
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73f7bd115b994bb86590098ba14d49c9
https://doi.org/10.1002/chin.199142129
https://doi.org/10.1002/chin.199142129
Publikováno v:
ChemInform. 23
Thermolysis of enynes with pentacarbonyl(butylmethoxycarbene)molybdenum (0) 1a produces vinylcyclopropanes in significantly higher yields than the analogous chromium carbene complexes 1b and 3. Additionally, enynes with an allylic ether substituent a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd2a66370479d57328d460e9e3a5fb93
https://doi.org/10.1002/chin.199226075
https://doi.org/10.1002/chin.199226075
Publikováno v:
ChemInform. 24
It has been observed that the reaction of 1,6- and 1,7-enynes with pentacarbonyl(butylmethoxycarbene)molybdenum(0) (18) produces vinylcyclopropanes in good to excellent yield. A systematic investigation into the factors which govern the success of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ffa7cdc325ddfbddc503dd0c15c42a7
https://doi.org/10.1002/chin.199308109
https://doi.org/10.1002/chin.199308109
Publikováno v:
Journal of the American Chemical Society. 114:8424-8434
It has been observed that the reaction of 1,6- and 1,7-enynes with pentacarbonyl(butylmethoxycarbene)molybdenum(0) (18) produces vinylcyclopropanes in good to excellent yield. A systematic investigation into the factors which govern the success of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af1b79efcb74e85a1b28918a0e75f426
https://doi.org/10.1021/ja00048a012
https://doi.org/10.1021/ja00048a012
Publikováno v:
Tetrahedron Letters. 32:6311-6314
Thermolysis of enynes with pentacarbonyl(butylmethoxycarbene)molybdenum (0) 1a produces vinylcyclopropanes in significantly higher yields than the analogous chromium carbene complexes 1b and 3. Additionally, enynes with an allylic ether substituent a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f56df42e5773a93cd514b2a244337a
https://doi.org/10.1016/0040-4039(91)80155-y
https://doi.org/10.1016/0040-4039(91)80155-y
Publikováno v:
Protein Microarray Technology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fae95ccd964a31db9fb9dfc2a3f4d00
https://doi.org/10.1002/3527601554.ch3
https://doi.org/10.1002/3527601554.ch3
Autor:
Karin A. Hughes, Robert J. Kaiser, Jean P. Wiley, Mark L. Stolowitz, Edward A. Kesicki, Kevin P. Lund
Publikováno v:
Bioconjugate chemistry. 12(2)
Phenylboronic acid bioconjugates prepared from alkaline phosphatase by reaction with either 2,5-dioxopyrrolidinyl 3-[N-[3-(1,3,2-dioxaboran-2-yl)phenyl]carbamoyl]propanoate (PBA-XX-NHS) or 2,5-dioxopyrrolidinyl 6-[[3,5-di-(1,3,2-dioxaboran-2-yl)pheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce92df5a3fc8aaebbb8fd79dbe59e595
https://pubmed.ncbi.nlm.nih.gov/11312685
https://pubmed.ncbi.nlm.nih.gov/11312685