Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Laura S. Kocsis"'
Publikováno v:
Rubber Chemistry and Technology. 90:325-336
The influence of stereochemistry of polar modifiers on the microstructure of polybutadiene and poly(styrene-co-butadiene) was evaluated for 2,2′-ditetrahydrofurylpropane (DTHFP). The meso and d,l diastereomers were isolated from commercial 50/50 mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9656efe11c636b63de9399aad6d55a93
https://doi.org/10.5254/rct.17.82692
https://doi.org/10.5254/rct.17.82692
Autor:
Kay M. Brummond, Laura S. Kocsis
Publikováno v:
Accounts of Chemical Research. 48:2320-2329
Reaction discovery plays a vital role in accessing new chemical entities and materials possessing important function.1 In this Account, we delineate our reaction discovery program regarding the [4 + 2] cycloaddition reaction of styrene-ynes. In parti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc5075f7b354f7afe1f7ea8ecb4d7efd
https://doi.org/10.1021/acs.accounts.5b00126
https://doi.org/10.1021/acs.accounts.5b00126
Autor:
Stefan Bernhard, Bhaskar Godugu, Laura S. Kocsis, Kay M. Brummond, Husain N. Kagalwala, Sharlene Mutto, Dean J. Tantillo
Publikováno v:
The Journal of Organic Chemistry. 80:11686-11698
The Diels-Alder reaction represents one of the most thoroughly studied and well-understood synthetic transformations for the assembly of six-membered rings. Although intramolecular dehydro-Diels-Alder (IMDDA) reactions have previously been employed f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba6964d47eae55f8a7bdcdd06854e6ec
https://doi.org/10.1021/acs.joc.5b00200
https://doi.org/10.1021/acs.joc.5b00200
Autor:
Kay M. Brummond, Laura S. Kocsis
Publikováno v:
Organic Letters
Intramolecular dehydro-Diels–Alder (DDA) reactions are performed affording arylnaphthalene or aryldihydronaphthalene lactones selectively as determined by choice of reaction solvent. This constitutes the first report of an entirely selective format
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238019c2b1d7ea625a788fec9811806d
https://doi.org/10.1021/ol501853y
https://doi.org/10.1021/ol501853y
Publikováno v:
Organic Letters. 15:2578-2581
The synthesis and utility of attachable cyclopenta[b]naphthalene solvatochromic fluorophores related to Prodan are described. Two fluorophores were selected for functionalization and bioconjugation studies. The skeletons were chemically modified to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d1c512c1e625185f9eeab4b89b72fa
https://doi.org/10.1021/ol400292q
https://doi.org/10.1021/ol400292q
Publikováno v:
Journal of the American Chemical Society. 134:12418-12421
The synthesis and photophysical properties of a series of naphthalene-containing solvatochromic fluorophores are described within. These novel fluorophores are prepared using a microwave-assisted dehydrogenative Diels-Alder reaction of styrene, follo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::679be20f7fb8a5e00c23675165e819e5
https://doi.org/10.1021/ja3055029
https://doi.org/10.1021/ja3055029
Autor:
Deborah Galinis, Sheila J. Miknyoczki, Ted L. Underiner, Damaris Rolon-Steele, Jean Husten, Craig A. Zificsak, Thelma S. Angeles, Torsten Herbertz, Mark S. Albom, Bruce D. Dorsey, Laura S. Kocsis, Kevin J. Wells-Knecht, Jay P. Theroff, Lisa D. Aimone, Kelli S. Zeigler, Candace S. Worrell, Rebecca A. Brown, Christine LoSardo, Seetha Murthy, Jennifer Grobelny
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:660-663
Elaboration of the SAR around a series of 2,4-diaminopyrimidines led to a number of c-Met inhibitors in which kinase selectivity was modulated by substituents appended on the C4-aminobenzamide ring and the nature of the C2-aminoaryl ring. Further lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2f5ede7c3bb696001314f924df06f4
https://doi.org/10.1016/j.bmcl.2010.12.013
https://doi.org/10.1016/j.bmcl.2010.12.013
Autor:
Emmanuel A. Theodorakis, Kristyna M. Elbel, Kay M. Brummond, Billie A. Hardigree, Laura S. Kocsis, Mark A. Haidekker
Publikováno v:
Kocsis, LS; Elbel, KM; Hardigree, BA; Brummond, KM; Haidekker, MA; & Theodorakis, EA. (2015). Cyclopenta[b]naphthalene cyanoacrylate dyes: Synthesis and evaluation as fluorescent molecular rotors. Organic and Biomolecular Chemistry, 13(10), 2965-2973. doi: 10.1039/c4ob02563f. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/7gs2m6s1
Organic & biomolecular chemistry, vol 13, iss 10
Organic & biomolecular chemistry, vol 13, iss 10
© 2015 The Royal Society of Chemistry. We describe the design, synthesis and fluorescent profile of a family of environment-sensitive dyes in which a dimethylamino (donor) group is conjugated to a cyanoacrylate (acceptor) unit via a cyclopenta[b]nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ad2dfce28d71464c90e8b4c339111d
https://europepmc.org/articles/PMC4339457/
https://europepmc.org/articles/PMC4339457/
Autor:
Kay M. Brummond, Laura S. Kocsis
Publikováno v:
ChemInform. 46
Depending on the choice of the reaction solvent the microwave promoted intramolecular Diels—Alder reaction of cinnamyl esters of arylpropiolic acids [cf.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d418ef6566b02813546c0ba2710e4d76
https://doi.org/10.1002/chin.201507031
https://doi.org/10.1002/chin.201507031
Publikováno v:
Journal of Visualized Experiments.
Functionalized naphthalenes have applications in a variety of research fields ranging from the synthesis of natural or biologically active molecules to the preparation of new organic dyes. Although numerous strategies have been reported to access nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b10e6111444f29ec1cf18a713f42f61
https://doi.org/10.3791/50511
https://doi.org/10.3791/50511