Zobrazeno 1 - 10
of 163
pro vyhledávání: '"Erik J. Sorensen"'
Autor:
Shishir Sharma, Jingyao Liu, Xue Zhang, Sangeeta Shrestha Sharma, Erik J. Sorensen, Matthias Bureik
Publikováno v:
Biochemistry and Biophysics Reports, Vol 24, Iss , Pp 100861- (2020)
Activity of human CYP26A1 towards six proluciferin probe substrates and their ester derivatives was monitored. These included three monofluorobenzyl ether isomers and three five-membered heterocycles. Overall, luciferin substrates with a free acid gr
Externí odkaz:
https://doaj.org/article/38c2a22298074fc583a1f5a60190bb84
Autor:
Francisco de Asís Balaguer, Tobias Mühlethaler, Juan Estévez-Gallego, Enrique Calvo, Juan Francisco Giménez-Abián, April L. Risinger, Erik J. Sorensen, Christopher D. Vanderwal, Karl-Heinz Altmann, Susan L. Mooberry, Michel O. Steinmetz, María Ángela Oliva, Andrea E. Prota, J. Fernando Díaz
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 6, p 1392 (2019)
It has been proposed that one of the mechanisms of taxane-site ligand-mediated tubulin activation is modulation of the structure of a switch element (the M-loop) from a disordered form in dimeric tubulin to a folded helical structure in microtubules.
Externí odkaz:
https://doaj.org/article/abae6ee18f044a3685a5886a0f71911a
Autor:
Nicholas A. Falcone, Aaron T. Bosse, Hojoon Park, Jin-Quan Yu, Huw M. L. Davies, Erik J. Sorensen
Publikováno v:
Organic Letters. 23:9393-9397
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4fee13c86b9e1d7a8736f9fd846abc1
https://doi.org/10.1021/acs.orglett.1c03502
https://doi.org/10.1021/acs.orglett.1c03502
Autor:
Xiangyang Chen, Jonathan L. Wong, Philip A. Provencher, John F. Hoskin, Erik J. Sorensen, Jin-Quan Yu, Kendall N. Houk
Publikováno v:
Journal of the American Chemical Society. 143:20035-20041
Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)-H arylation of ketones. The rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8e4688c3b1a84a1ded34e14f40538cc
https://doi.org/10.1021/jacs.1c09368
https://doi.org/10.1021/jacs.1c09368
Autor:
Erik J. Sorensen, Philip A. Provencher, John F. Hoskin, Katherine L. Bay, Kendall N. Houk, Jin-Quan Yu
Publikováno v:
ACS Catalysis. 11:3115-3127
We report Pd(II)-catalyzed cyclative C(sp3)–H arylation of ketones with a transient directing group (TDG). Based on calculations, the oxidative addition step implicates a highly strained trigonal b...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a69eb8edd1b5415574e935c7c2ab91d
https://doi.org/10.1021/acscatal.0c05081
https://doi.org/10.1021/acscatal.0c05081
Publikováno v:
Applied Biochemistry and Biotechnology. 193:218-237
We report the synthesis of seven new proluciferins for convenient activity determination of enzymes belonging to the cytochrome P450 (CYP) 4 family. Biotransformation of these probe substrates was monitored using each of the twelve human CYP4 family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee1f1a0949ace6b306a8b075dede27cc
https://doi.org/10.1007/s12010-020-03388-6
https://doi.org/10.1007/s12010-020-03388-6
Publikováno v:
Organic Letters. 22:1791-1795
Metal carbenes, derived from the decomposition of diazo compounds, are valued for their capacity to perform a variety of transformations. A unique class of acyclic, bis-diazo compounds, the donor-acceptor-acceptor 1,3-bisdiazo compounds, are describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::855b7a70357d05927d5dbe9aa79f5503
https://doi.org/10.1021/acs.orglett.0c00103
https://doi.org/10.1021/acs.orglett.0c00103
Autor:
Nicholas A, Falcone, Aaron T, Bosse, Hojoon, Park, Jin-Quan, Yu, Huw M L, Davies, Erik J, Sorensen
Publikováno v:
Organic letters. 23(24)
An enantioselective formal synthesis of (-)-aflatoxin B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9abf23c843a6409921fcf8d3b9ca466d
https://pubmed.ncbi.nlm.nih.gov/34865494
https://pubmed.ncbi.nlm.nih.gov/34865494
Autor:
Philip A, Provencher, John F, Hoskin, Jonathan J, Wong, Xiangyang, Chen, Jin-Quan, Yu, K N, Houk, Erik J, Sorensen
Publikováno v:
Journal of the American Chemical Society. 143(48)
Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d41cb68834557e699d4cb44566319b7
https://pubmed.ncbi.nlm.nih.gov/34817163
https://pubmed.ncbi.nlm.nih.gov/34817163
Autor:
Erik J. Sorensen, Philip A. Provencher, Jin-Quan Yu, Kendall N. Houk, John F. Hoskin, Xiangyang Chen, Jonathan L. Wong
Methylene-selective C‒H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) cataly-sis. In this paper we report a Pd(II) catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)‒H arylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7230d3902742127c776180e10442d9ba
https://doi.org/10.33774/chemrxiv-2021-kq8np-v2
https://doi.org/10.33774/chemrxiv-2021-kq8np-v2
