Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Peter H. Fuller"'
Autor:
David A. Candito, Vladimir Simov, Anmol Gulati, Solomon Kattar, Ryan W. Chau, Blair T. Lapointe, Joey L. Methot, Duane E. DeMong, Thomas H. Graham, Ravi Kurukulasuriya, Mitchell H. Keylor, Ling Tong, Gregori J. Morriello, John J. Acton, Barbara Pio, Weiguo Liu, Jack D. Scott, Michael J. Ardolino, Theodore A. Martinot, Matthew L. Maddess, Xin Yan, Hakan Gunaydin, Rachel L. Palte, Spencer E. McMinn, Lisa Nogle, Hongshi Yu, Ellen C. Minnihan, Charles A. Lesburg, Ping Liu, Jing Su, Laxminarayan G. Hegde, Lily Y. Moy, Janice D. Woodhouse, Robert Faltus, Tina Xiong, Paul Ciaccio, Jennifer A. Piesvaux, Karin M. Otte, Matthew E. Kennedy, David Jonathan Bennett, Erin F. DiMauro, Matthew J. Fell, Santhosh Neelamkavil, Harold B. Wood, Peter H. Fuller, J. Michael Ellis
Publikováno v:
Journal of Medicinal Chemistry. 65:16801-16817
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::365ba0e1a6a6d085b4344b637344b726
https://doi.org/10.1021/acs.jmedchem.2c01605
https://doi.org/10.1021/acs.jmedchem.2c01605
Autor:
David A. Evans, Jason J. Beiger, Jason D. Burch, Peter H. Fuller, Frank Glorius, Egmont Kattnig, David A. Thaisrivongs, William C. Trenkle, Joseph M. Young, Jing Zhang
Publikováno v:
Journal of the American Chemical Society. 144(43)
The total syntheses of aflastatin A and its C3-C48 degradation fragment (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b3d80d5f297311efb9898f59054d005
https://pubmed.ncbi.nlm.nih.gov/36269121
https://pubmed.ncbi.nlm.nih.gov/36269121
Autor:
Mitchell H. Keylor, Anmol Gulati, Solomon D. Kattar, Rebecca E. Johnson, Ryan W. Chau, Kaila A. Margrey, Michael J. Ardolino, Cayetana Zarate, Kelsey E. Poremba, Vladimir Simov, Gregori J. Morriello, John J. Acton, Barbara Pio, Xin Yan, Rachel L. Palte, Spencer E. McMinn, Lisa Nogle, Charles A. Lesburg, Donovon Adpressa, Shishi Lin, Santhosh Neelamkavil, Ping Liu, Jing Su, Laxminarayan G. Hegde, Janice D. Woodhouse, Robert Faltus, Tina Xiong, Paul J. Ciaccio, Jennifer Piesvaux, Karin M. Otte, Harold B. Wood, Matthew E. Kennedy, David Jonathan Bennett, Erin F. DiMauro, Matthew J. Fell, Peter H. Fuller
Publikováno v:
Journal of medicinal chemistry. 65(1)
The leucine-rich repeat kinase 2 (LRRK2) protein has been genetically and functionally linked to Parkinson's disease (PD), a disabling and progressive neurodegenerative disorder whose current therapies are limited in scope and efficacy. In this repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6720c280fccf3e18653a864a196348ad
https://pubmed.ncbi.nlm.nih.gov/34967623
https://pubmed.ncbi.nlm.nih.gov/34967623
Publikováno v:
ChemInform. 40
The copper-catalyzed enantioselective intramolecular aminooxygenation of alkenes is reported herein. This is the first report of an enantioselective intramolecular alkene aminooxygenation process. N-Arylsulfonyl-2-allylanilines and 4-pentenylarylsulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::942ff41bcc713555408ec72925223b69
https://doi.org/10.1002/chin.200921108
https://doi.org/10.1002/chin.200921108
The copper-catalyzed enantioselective intramolecular aminooxygenation of alkenes is reported herein. This is the first report of an enantioselective intramolecular alkene aminooxygenation process. N-Arylsulfonyl-2-allylanilines and 4-pentenylarylsulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558c33ebc6f9488f3cb0bf4d11d32de6
https://europepmc.org/articles/PMC2674573/
https://europepmc.org/articles/PMC2674573/
Autor:
Peter H. Fuller, Sherry R. Chemler
Publikováno v:
ChemInform. 39
The copper(II) carboxylate-promoted intramolecular carboamination reactions of variously substituted gamma-alkenyl amides have been investigated. These oxidative cyclization reactions efficiently provide polycyclic lactams, useful intermediates in ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1389fe5ef4a5da573f973b61f7274be6
https://doi.org/10.1002/chin.200822123
https://doi.org/10.1002/chin.200822123
Autor:
Peter H. Fuller, Sherry R. Chemler
Publikováno v:
Organic letters. 9(26)
The copper(II) carboxylate-promoted intramolecular carboamination reactions of variously substituted gamma-alkenyl amides have been investigated. These oxidative cyclization reactions efficiently provide polycyclic lactams, useful intermediates in ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff0d3a827994d0183885f653c1d7013c
https://pubmed.ncbi.nlm.nih.gov/18044907
https://pubmed.ncbi.nlm.nih.gov/18044907
Autor:
Peter H. Fuller, Sherry R. Chemler
Publikováno v:
ChemInform. 38
The de nouvo synthesis of small organic heterocyclic molecules has benefited from recent protocols for copper-facilitated additions of heteroatoms to alkenes, alkynes and arenes. This tutorial review summarizes a number of these recent contributions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc93b1051587e2c76e25feb46e63c7cf
https://doi.org/10.1002/chin.200743243
https://doi.org/10.1002/chin.200743243
Publikováno v:
ChemInform. 38
An expanded substrate scope and in-depth analysis of the reaction mechanism of the copper(II) carboxylate-promoted intramolecular carboamination of unactivated alkenes is described. This method pro...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1563c69999d8308b8819ae0755bfe4a6
https://doi.org/10.1002/chin.200737119
https://doi.org/10.1002/chin.200737119
Publikováno v:
The Journal of organic chemistry. 72(10)
An expanded substrate scope and in-depth analysis of the reaction mechanism of the copper(II) carboxylate-promoted intramolecular carboamination of unactivated alkenes is described. This method provides access to N-functionalized pyrrolidines and pip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ec68f7a2367dc74ef45ae66859831f
https://pubmed.ncbi.nlm.nih.gov/17428100
https://pubmed.ncbi.nlm.nih.gov/17428100