Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Debora Chiodi"'
Autor:
Debora Chiodi, Yoshihiro Ishihara
Publikováno v:
Journal of Medicinal Chemistry. 66:5305-5331
Chlorine is one of the most common atoms present in small-molecule drugs beyond carbon, hydrogen, nitrogen and oxygen. There are currently more than 250 FDA-approved chlorine-containing drugs, yet the beneficial effect of the chloro substituent has n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::add054a438562707d4a4fc18d15e4321
https://doi.org/10.1021/acs.jmedchem.2c02015
https://doi.org/10.1021/acs.jmedchem.2c02015
Autor:
You-Chen Lin, Fabian Schneider, Kelly J. Eberle, Debora Chiodi, Hugh Nakamura, Solomon H. Reisberg, Jason Chen, Masato Saito, Phil S. Baran
Publikováno v:
Journal of the American Chemical Society. 144:14458-14462
A concise, modular synthesis of the novel antibiotic darobactin A is disclosed. The synthesis successfully forges the hallmark strained macrocyclic ring systems in a sequential fashion. Key transformations include two atroposelective Larock-based mac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea7939a6f7c5118e6f9934070ad2040
https://doi.org/10.1021/jacs.2c05892
https://doi.org/10.1021/jacs.2c05892
Autor:
You-Chen Lin, Fabian Schneider, Kelly Eberle, Debora Chiodi, Hugh Nakamura, Solomon Reisberg, Jason Chen, masato saito, phil baran
A concise, modular synthesis of the novel antibiotic darobactin A is disclosed. The synthesis successfully forges the hallmark strained macrocyclic ring systems in a sequential fashion. Key transformations include two atroposelective Larock-macrocyli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebba63fb90caff241dcbc8e8f5a33779
https://doi.org/10.26434/chemrxiv-2022-28tbx
https://doi.org/10.26434/chemrxiv-2022-28tbx
Autor:
Pengfei Hu, Tianhua Tang, Chi He, Moses G. Gichinga, Phil S. Baran, Sameer Tyagi, Shelley D. Minteer, Rafael Navratil, Debora Chiodi, Masato Saito, Massimiliano Lamberto, Michael Meanwell, Matthew S. Sigman, Mayank Tanwar, Matthew Neurock, Martin D. Eastgate, Bruce P. McKillican, Michael A. Schmidt, Longrui Chen, Sagar Udyavara, Christian A. Malapit, Ethan Carlson, Cian Kingston, Yu Kawamata
Publikováno v:
J Am Chem Soc
The site-specific oxidation of strong C(sp(3))–H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::230d8758f39c29311d5370d2f48682a0
https://doi.org/10.1021/jacs.1c03780
https://doi.org/10.1021/jacs.1c03780
Autor:
Ahmed Anwar Dezaye, Sirwan T. Othman, Giuseppe Zanoni, Alessio Porta, Debora Chiodi, Emanuele Casali
Publikováno v:
The Journal of Organic Chemistry
A novel approach for the formation of anomeric carbon-functionalized furanoside systems was accomplished through the employment of an oxo-rhenium catalyst. The transformation boasts a broad range of nucleophiles including allylsilanes, enol ethers, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db5ed03e52d52fda2df38b7ea00a879b
http://europepmc.org/articles/PMC8279489
http://europepmc.org/articles/PMC8279489
Autor:
Matthew Neurock, Michael A. Schmidt, Cian Kingston, Bruce P. McKillican, Masato Saito, Debora Chiodi, Chi He, Rafael Navratil, Michael Meanwell, Moses G. Gichinga, Max Lamberto, Shelley D. Minteer, Sagar Udyavara, Mayank Tanwar, Christian A. Malapit, Yu Kawamata, Martin D. Eastgate, Longrui Chen, Ethan Carlson, Matthew S. Sigman, Pengfei Hu, Tianhua Tang, Phil S. Baran, Sameer Tyagi
The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organicsynthesis. From simplifying access to metabolites and late-stage diversification of lead compoundsto truncating retrosynthetic plans, there is a growing need for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7470d5850e22aaad592fc1a940e57b50
https://doi.org/10.26434/chemrxiv.14054783.v1
https://doi.org/10.26434/chemrxiv.14054783.v1