Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Evan O. Romero"'
Autor:
Evan O. Romero, Anthony T. Saucedo, José R. Hernández-Meléndez, Di Yang, Suman Chakrabarty, Alison R. H. Narayan
Publikováno v:
JACS Au, Vol 3, Iss 8, Pp 2073-2085 (2023)
Externí odkaz:
https://doaj.org/article/be82e76fffa949c8b490f3dc05c329e8
Publikováno v:
ACS Central Science, Vol 7, Iss 7, Pp 1105-1116 (2021)
Externí odkaz:
https://doaj.org/article/4864285d3e144546b78d29bdec88e030
Autor:
Evan O. Romero, Jonathan C. Perkins, Jessica E. Burch, David A. Delgadillo, Hosea M. Nelson, Alison R. H. Narayan
Publikováno v:
Organic Letters. 25:1547-1552
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99e8c89520d6e9c559bb745ed5435061
https://doi.org/10.1021/acs.orglett.3c00334
https://doi.org/10.1021/acs.orglett.3c00334
Autor:
John R. Sowa, Scott A. Savage, Eric M. Simmons, Martin D. Eastgate, Yichen Tan, Evan O. Romero, Steven R. Wisniewski, R. Erik Plata, Donna G. Blackmond
Publikováno v:
The Journal of Organic Chemistry. 84:7961-7970
A mechanistic study on a direct arylation using a native picolylamine directing group is reported. Kinetic studies determined the concentration dependence of substrates and catalysts, as well as catalyst degradation, which led to the development of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de9f3c3915a959ba16317bc25faa77d8
https://doi.org/10.1021/acs.joc.9b00823
https://doi.org/10.1021/acs.joc.9b00823
Publikováno v:
Acc Chem Res
The total synthesis of structurally complex natural products has challenged and inspired generations of chemists and remains an exciting area of active research. Despite their history as privileged bioactivity-rich scaffolds, the use of natural produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4aa4fb51739d1358d6ca97bd8683b60
https://pubmed.ncbi.nlm.nih.gov/33600149
https://pubmed.ncbi.nlm.nih.gov/33600149
Autor:
Steven R. Wisniewski, Scott A. Savage, Jason M. Stevens, Miao Yu, Kenneth J. Fraunhoffer, Evan O. Romero
Publikováno v:
The Journal of Organic Chemistry. 84:4704-4714
BMS-919373 is a highly functionalized quinazoline under investigation as a selective, potent IKur current blocker. By utilizing the aminomethylpyridine side chain at C-4, a selective C–H functionalization at C-5 was invented, enabling the efficient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c2c94c31df7308f3109f0ba82ac62f
https://doi.org/10.1021/acs.joc.8b02254
https://doi.org/10.1021/acs.joc.8b02254
Autor:
Connor P. Reidy, Evan O. Romero, Nicholas W. Vryhof, Andrea N. Bootsma, David C. Wierenga, Carolyn E. Anderson, Noah M. PreFontaine
Publikováno v:
The Journal of Organic Chemistry. 85:3990-3991
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7af4e21adf8827105c8eb1080c1aa9f
https://doi.org/10.1021/acs.joc.0c00151
https://doi.org/10.1021/acs.joc.0c00151
Autor:
Evan O. Romero, Paul M. Zimmerman, Kevin C Skinner, Summer A. Baker Dockrey, Jonathan C Perkins, Tyler J. Doyon, Alison R. H. Narayan
Publikováno v:
J Am Chem Soc
Generation of reactive intermediates and interception of these fleeting species under physiological conditions is a common strategy employed by Nature to build molecular complexity. However, selective formation of these species under mild conditions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7873ecc4285cbd0cf8600164cd24addd
https://europepmc.org/articles/PMC7193901/
https://europepmc.org/articles/PMC7193901/
Autor:
Tyler Doyon, Jonathan Perkins, Summer A. Baker Dockrey, Evan O. Romero, Kevin Skinner, Paul M. Zimmerman, Alison Narayan
Generation of reactive intermediates and interception of these fleeting species in a cascade is a common strategy employed by Nature. However, formation of these species under mild conditions using traditional synthetic techniques can present a chall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d708646294a5a2f4c8a213c99906d52
https://doi.org/10.26434/chemrxiv.7828769.v3
https://doi.org/10.26434/chemrxiv.7828769.v3
Autor:
Leslie A. Nickerson, Evan O. Romero, Jaimie E. Van de Burg, Colin T. Hartgerink, Emily E. Zerull, Matthew D. Rossler, Richard J. Staples, Miles M. Mason, Abigail K. Frndak, Carolyn E. Anderson, Benjamin L. Boss
Publikováno v:
Organic letters. 21(14)
A new Au(I)-catalyzed method for the preparation of trisubstituted indolizines from easily accessible 2-propargyloxy-pyridines is reported. The reaction tolerates a wide range of functionality, allowing for diversity to be introduced in four distinct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc6febf619259bde9f4195a7a044111f
https://pubmed.ncbi.nlm.nih.gov/31260323
https://pubmed.ncbi.nlm.nih.gov/31260323