About: Kay M. Brummond

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American synthetic chemist

Attributes	Values
rdf:type	Item
description	연구원 (ko) wetenschapper (nl) дослідниця (uk) изилдөөчү (ky) American synthetic chemist (en)
rdfs:label	Kay M Brummond (nl) Kay M. Brummond (en)
skos:prefLabel	Kay M Brummond (nl) Kay M. Brummond (en)
name	Kay M Brummond (nl) Kay M. Brummond (en)
given name	wds:Q89427466-e706c088-4cfc-6af6-a8b4-e1bea014cb9d
given name	Kay
instance of	wds:Q89427466-2B77DAA9-A77D-49E7-A399-8CCA136BD788
instance of	Homo sapiens
award received	wds:Q89427466-4e6c3da7-4ce5-f99a-a4fc-d1edfa5553da wds:Q89427466-6baf216b-4014-b313-69a4-2455adebefa5
award received	ACS Award for Encouraging Women into Careers in the Chemical Sciences Fellow of the American Association for the Advancement of Science
Academic Tree ID	wds:Q89427466-70515acb-40df-4f57-6aa9-3edde6b3017e
Google Knowledge Graph ID	wds:Q89427466-F8A747C4-5C70-4A2F-9539-AEA759833193
Google Knowledge Graph ID	http://g.co/kg/g/11bwfvpvmr
Academic Tree ID	72553
Google Knowledge Graph ID	/g/11bwfvpvmr
ResearchGate profile ID	wds:Q89427466-8b1a439f-4904-2de1-290c-78c5e072a012
ResearchGate profile ID	Kay-Brummond
Google Scholar author ID	wds:Q89427466-266abb6b-4a38-05cb-ccc3-539c0be554c6
Google Scholar author ID	6iI4MkEAAAAJ
skos:altLabel	K M Brummond (en) K. M. Brummond (en) K.M. Brummond (en) KM Brummond (en) Kay Brummond (en) Kay M Brummond (en) Kay Michille Brummond (en)
occupation	wds:Q89427466-20FB1EBB-E05A-48A0-944B-F408814AB10C
employer	wds:Q89427466-7d277e21-43da-f099-ea88-5775ea973af7
sex or gender	wds:Q89427466-f09c5dbc-99db-4e26-9861-226cf0d18ea2
VIAF ID	wds:Q89427466-b2b783d0-088b-4c13-8a54-6541c0c6652f
GND ID	wds:Q89427466-3514405e-458d-a25a-d663-84a000544fb1 wds:Q89427466-e0e5c50c-46f0-6914-a966-2c962d4d56ca
country of citizenship	wds:Q89427466-764f73cb-4a99-1fc4-6a90-79e8018847b8
educated at	wds:Q89427466-0D2ED57B-8052-42C4-A252-2365F92B9F6F wds:Q89427466-533dcd3e-462f-7a95-c5ab-f0c7d8b4c42b
family name	wds:Q89427466-8b8910be-4780-24b6-e9fe-0734ed97d411
VIAF ID	http://viaf.org/viaf/310590652
GND ID	https://d-nb.info/gnd/105766510X https://d-nb.info/gnd/173973299
occupation	researcher
employer	University of Pittsburgh
sex or gender	female organism
VIAF ID	310590652
GND ID	105766510X 173973299
country of citizenship	United States of America
educated at	Pennsylvania State University University of Nebraska–Lincoln
family name	Brummond
ORCID iD	wds:Q89427466-F7B9EE81-9F44-46C9-A75A-51F3D1F5B181
ORCID iD	https://orcid.org/0000-0003-3595-6806
ORCID iD	0000-0003-3595-6806
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q89427466 Kay Brummond
is author of	A thermal dehydrogenative Diels-Alder reaction of styrenes for the concise synthesis of functionalized naphthalenes Structurally unique inhibitors of human mitogen-activated protein kinase phosphatase-1 identified in a pyrrole carboxamide library Cdc25B dual-specificity phosphatase inhibitors identified in a high-throughput screen of the NIH compound library Design and synthesis of a library of tetracyclic hydroazulenoisoindoles Allenes and transition metals: a diverging approach to heterocycles Intramolecular dehydro-Diels-Alder reaction affords selective entry to arylnaphthalene or aryldihydronaphthalene lignans Solid-Phase Synthesis of BRL 49653. Chemical methodology as a source of small-molecule checkpoint inhibitors and heat shock protein 70 (Hsp70) modulators Allene chemistry Unique strategy for the assembly of the carbon skeleton of guanacastepene A using an allenic Pauson-Khand-type reaction Alkyne Ligation Handles: Propargylation of Hydroxyl, Sulfhydryl, Amino, and Carboxyl Groups via the Nicholas Reaction A redox economical synthesis of bioactive 6,12-guaianolides. Complete transfer of chirality in an intramolecular, thermal [2 + 2] cycloaddition of allene-ynes to form non-racemic spirooxindoles A formal total synthesis of (-)-FR901483, using a tandem cationic aza-Cope rearrangement/Mannich cyclization approach Cyclopenta[b]naphthalene cyanoacrylate dyes: synthesis and evaluation as fluorescent molecular rotors Diverging Rh(I)-catalyzed carbocylization strategy to prepare a library of unique cyclic ethers Synthesis and photophysical properties of a series of cyclopenta[b]naphthalene solvatochromic fluorophores. Intramolecular didehydro-Diels-Alder reaction and its impact on the structure-function properties of environmentally sensitive fluorophores Mo(CO)6- and [Rh(CO)2Cl]2-catalyzed allenic cyclocarbonylation reactions of alkynones: efficient access to bicyclic dienediones PHOSPHINE-CATALYZED [4+2] ANNULATION: SYNTHESIS OF ETHYL 6-PHENYL-1-TOSYL-1,2,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLATE. Enantioselective synthesis of 5,7-bicyclic ring systems from axially chiral allenes using a Rh(I)-catalyzed cyclocarbonylation reaction Differentiating mechanistic possibilities for the thermal, intramolecular [2 + 2] cycloaddition of allene-ynes Toward a molecular understanding of the interaction of dual specificity phosphatases with substrates: insights from structure-based modeling and high throughput screening Diverging DOS strategy using an allene-containing tryptophan scaffold and a library design that maximizes biologically relevant chemical space while minimizing the number of compounds Rhodium(I)-catalyzed allenic carbocyclization reaction affording delta- and epsilon-lactams Mechanistic Insight into the Dehydro-Diels-Alder Reaction of Styrene-Ynes. Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions A rhodium(I)-catalyzed formal allenic Alder ene reaction for the rapid and stereoselective assembly of cross-conjugated trienes Synthesis and in silico screening of a library of β-carboline-containing compounds The first total synthesis of 15-deoxy-Delta12,14-prostaglandin J2 and the unambiguous assignment of the C14 stereochemistry Rhodium(I)-catalyzed ene-allene carbocyclization strategy for the formation of azepines and oxepines Microwave-assisted intramolecular [2 + 2] Allenic cycloaddition reaction for the rapid assembly of bicyclo[4.2.0]octa-1,6-dienes and bicyclo[5.2.0]nona-1,7-dienes Solution-phase synthesis of a tricyclic pyrrole-2-carboxamide discovery library applying a stetter-Paal-Knorr reaction sequence Heterocyclic alpha-alkylidene cyclopentenones obtained via a Pauson-Khand reaction of amino acid derived allenynes. A scope and limitation study directed toward the preparation of a tricyclic pyrrole library Identification of ATR-Chk1 pathway inhibitors that selectively target p53-deficient cells without directly suppressing ATR catalytic activity An allenic Pauson-Khand approach to 6,12-guaianolides

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