Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Frederick J. Lakner"'
Autor:
Mathew P.D. Mahindaratne, Brian A. Quiñones, Antonio Recio III, Erik A. Rodriguez, Frederick J. Lakner, George R. Negrete
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 321-328 (2005)
Externí odkaz:
https://doaj.org/article/dc27ae2cd5bc4b5f959e0e11683de637
Autor:
Ande Bao, Maritza V. Quintero, George R. Negrete, William T. Phillips, Beth A. Goins, Adelphe M. Mfuh, Mathew P. D. Mahindaratne, Frederick J. Lakner
Publikováno v:
Langmuir. 27:4447-4455
A novel asparagine-derived lipid analogue (ALA(11,17)) bearing a tetrahydropyrimidinone headgroup and two fatty chains (11 and 17 indicate the lengths of linear alkyl groups) was synthesized in high yield and purity. The thin film hydration of formul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac7c3a263211addeaacc4a3da94a50e2
https://doi.org/10.1021/la105085k
https://doi.org/10.1021/la105085k
Autor:
Boris V. Rogovoy, Alexander V. Ivachtchenko, Matthew A. Parker, Frederick J. Lakner, Alexander Viktorovich Khvat
Publikováno v:
Synthesis. 2009:1987-1990
Imidazolines substituted at the 1- and either the 4-, or 5-position with phenyl and at the 2-position with alkyl or phenyl have been prepared in racemic form. They appear to be fairly stable compounds and potentially useful as scaffolds in medicinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30b6a4bddad89d70941fca270664e46f
https://doi.org/10.1055/s-0029-1216784
https://doi.org/10.1055/s-0029-1216784
Autor:
Frederick J. Lakner, Brian A. Quiñones, Eric A. Rodriguez, Antonio Recio, Mathew P. D. Mahindaratne, George R. Negrete
Publikováno v:
Tetrahedron. 61:9495-9501
Results are reported on the salt, concentration, and temperature effects in an aqueous, auxiliary-mediated asymmetric Diels–Alder cycloaddition. The auxiliaries were prepared under basic aqueous conditions from asparagine and trimethylacetaldehyde,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f87940c4a53ebb3f44bb9eb496cc783
https://doi.org/10.1016/j.tet.2005.08.003
https://doi.org/10.1016/j.tet.2005.08.003
Autor:
Brian A. Quiñones, Frederick J. Lakner, Eric A. Rodriguez, Antonio Recio, Mathew P. D. Mahindaratne, George R. Negrete
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 321-328 (2005)
A fully-telescoped, aqueous, auxiliary-mediated Diels-Alder cycloaddition in moderate selectivity is reported. The auxiliary is prepared from L-asparagine and trimethylacetaldehyde, and coupled without isolation to the acryloyl substrate. Direct addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb690a5ef900355a59549c253366f4c
https://doi.org/10.3998/ark.5550190.0006.627
https://doi.org/10.3998/ark.5550190.0006.627
Autor:
Kathy G. Jahangiri, Michael K. Dalton, Haiji Xia, Jeffrey R. Hammaker, Azra Pervin, Alexandre V. Ivachtchenko, Frederick J. Lakner, Alexander Viktorovich Khvat, Alexander S. Kiselyov
Publikováno v:
Tetrahedron Letters. 46:5325-5328
Novel mesoionic heterocyclic structures 8 have been obtained via the internal cyclization of thio- and amino-acid derivatives of 6-azauracil 7b–d . These compounds undergo ring-opening reactions with amines to yield the respective 6-azauracil amide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ac77a2d12585b41c638afa30ad4db23
https://doi.org/10.1016/j.tetlet.2005.06.032
https://doi.org/10.1016/j.tetlet.2005.06.032
Publikováno v:
Organic Letters. 15:2598-2600
A new route to the ergoline skeleton has been developed that does not require prior functionalization of the indole 4-position. The indole nucleus is introduced late in the synthesis to allow for eventual efficient introduction of substituents in thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7783fc5d7bfe2be37a8be8561062cc2c
https://doi.org/10.1021/ol400620a
https://doi.org/10.1021/ol400620a
Autor:
Coleman Gross, Bishwajit Nag, Satyanarayana Medicherla, Lesley B Pickford, Debendranath Dey, Frederick J. Lakner, Maya S. Gowri, Somesh Sharma, Partha Neogi, Jin Cheng
Publikováno v:
Bioorganic & Medicinal Chemistry. 11:4059-4067
A number of 2,4-thiazolidinedione derivatives of -phenyl substituted cinnamic acid were synthesized and studied for their PPAR agonist activity. The E-isomer of cinnamic acid, 11, showed moderate PPAR transactivation. The corresponding Z-isomer, 23,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64e8b5b166ba0bab9fa695d795b01f53
https://doi.org/10.1016/s0968-0896(03)00393-6
https://doi.org/10.1016/s0968-0896(03)00393-6
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 9:107-111
The stereochemistry of the chloroperoxidase-catalyzed epoxidation of indene has been elucidated. In aqueous solution the intial epoxide product is not stable and opens to form the cis-trans diols. When the reaction was carried out in the absence of w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e61fde97bdb3e15dd887d51e32408921
https://doi.org/10.1016/s1381-1177(99)00118-6
https://doi.org/10.1016/s1381-1177(99)00118-6
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 5:95-101
Recent experiments from several laboratories have shown that chloroperoxidase is able to catalyze a broad spectrum of stereoselective hydroxylation, sulfoxidation and epoxidation reactions. Our laboratory has investigated the substrate specificity of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e24dea24301265579f4c5e10def5bebf
https://doi.org/10.1016/s1381-1177(98)00013-7
https://doi.org/10.1016/s1381-1177(98)00013-7