A. Michael Downey - Publications
Affiliations: | Institute of Organic Chemistry and Biochemistry |
Area:
Tuberculosis, nucleos(t)ides, carbohydrates, phosphonates, medicinal chemistryWebsite:
http://www.uochb.cas.cz/hocekgroup/members/downey.htmlYear | Citation | Score | |||
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2021 | Zasłona ME, Downey AM, Seeberger PH, Moscovitz O. Semi- and fully synthetic carbohydrate vaccines against pathogenic bacteria: recent developments. Biochemical Society Transactions. PMID 34495299 DOI: 10.1042/BST20210766 | 0.325 | |||
2019 | Downey AM, Kapłonek P, Seeberger PH. MAIT Cells As Attractive Vaccine Targets. Febs Letters. PMID 31206659 DOI: 10.1002/1873-3468.13488 | 0.316 | |||
2017 | Downey AM, Hocek M. Strategies toward protecting group-free glycosylation through selective activation of the anomeric center. Beilstein Journal of Organic Chemistry. 13: 1239-1279. PMID 28694870 DOI: 10.3762/Bjoc.13.123 | 0.411 | |||
2017 | Downey AM, Pohl R, Roithova J, Hocek M. Synthesis of nucleosides through direct glycosylation of nucleobases with 5-O-mono-protected or 5-modified ribose. Improved protocol, scope and mechanism. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28112876 DOI: 10.1002/Chem.201604955 | 0.437 | |||
2015 | Downey AM, Richter C, Pohl R, Mahrwald R, Hocek M. Direct One-Pot Synthesis of Nucleosides from Unprotected or 5-O-Monoprotected d-Ribose. Organic Letters. 17: 4604-7. PMID 26355351 DOI: 10.1021/Acs.Orglett.5B02332 | 0.422 | |||
2014 | Downey AM, Cairo CW. Synthesis of α-brominated phosphonates and their application as phosphate bioisosteres Medchemcomm. 5: 1619-1633. DOI: 10.1039/C4Md00255E | 0.515 | |||
2013 | Downey AM, Cairo CW. α-Bromophosphonate analogs of glucose-6-phosphate are inhibitors of glucose-6-phosphatase. Carbohydrate Research. 381: 123-32. PMID 24095944 DOI: 10.1016/J.Carres.2013.08.003 | 0.508 | |||
2010 | Tulsi NS, Downey AM, Cairo CW. A protected l-bromophosphonomethylphenylalanine amino acid derivative (BrPmp) for synthesis of irreversible protein tyrosine phosphatase inhibitors. Bioorganic & Medicinal Chemistry. 18: 8679-86. PMID 21055952 DOI: 10.1016/J.Bmc.2010.09.040 | 0.514 | |||
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