Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Le Thanh Giang"'
Autor:
Le Thanh Giang, Fetter, József, Kajtár-Peredy, Mária, Lempert, Károly, Bertha, Ferenc, Keser″u, György M, Czira, Gábor, Czuppon, Tibor
Publikováno v:
In Tetrahedron 9 July 1999 55(28):8457-8474
Autor:
Zuegg, Johannes, Muldoon, Craig, Adamson, George, McKeveney, Declan, Le Thanh, Giang, Premraj, Rajaratnam, Becker, Bernd, Cheng, Mu, Elliott, Alysha G., Huang, Johnny X., Butler, Mark S., Bajaj, Megha, Seifert, Joachim, Singh, Latika, Galley, Nicola F., Roper, David I., Lloyd, Adrian J., Dowson, Christopher G., Cheng, Ting-Jen, Cheng, Wei-Chieh, Demon, Dieter, Meyer, Evelyne, Meutermans, Wim, Cooper, Matthew A.
Publikováno v:
Nature Communications
The rapid rise of multi-drug-resistant bacteria is a global healthcare crisis, and new antibiotics are urgently required, especially those with modes of action that have low-resistance potential. One promising lead is the liposaccharide antibiotic mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d4593292d865095e4494922e90301ea7
http://europepmc.org/articles/PMC4530474
http://europepmc.org/articles/PMC4530474
Autor:
Abbenante, Giovanni, Becker, Bernd, Blanc, Sébastien, Clark, Chris, Condie, Glenn, Fraser, Graeme, Grathwohl, Matthias, Halliday, Judy, Henderson, Senka, Lam, Ann, Liu, Ligong, Mann, Maretta, Muldoon, Craig, Pearson, Andrew, Premraj, Rajaratnam, Ramsdale, Tracie, Rossetti, Tony, Schafer, Karl, Le Thanh, Giang, Tometzki, Gerald, Vari, Frank, Verquin, Géraldine, Waanders, Jennifer, West, Michael, Wimmer, Norbert, Yau, Annika, Zuegg, Johannes, Meutermans, Wim
Publikováno v:
Journal of Medicinal Chemistry; 20240101, Issue: Preprints
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9925c8926f2cb5541276c72a8797d44b
https://doi.org/10.1002/chin.199646150
https://doi.org/10.1002/chin.199646150
Autor:
Gábor Czira, Le Thanh Giang, Mária Kajtár-Peredy, József Fetter, Antal Rockenbauer, Ildiko Nagy, László Korecz
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1131-1139
The majority of tetrazolylacetyl derivatives 2 and 7, when treated with lead tetraacetate in dry 1,4-dioxane at room or lower temperature, are oxidized with elimination of molecular nitrogen mainly to the corresponding alkynoyl derivatives 4 and 8, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64f8a90b11a4c9d77607438194939433
https://doi.org/10.1039/b005286h
https://doi.org/10.1039/b005286h
Publikováno v:
Tetrahedron. 55:13741-13748
1-(4-Methoxypheny])azetidin-2-ones 5a–5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a , 6b , 6c ' and 6d–6g . In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::775f4abfbfcaa83e5745be14a624f754
https://doi.org/10.1016/s0040-4020(99)00857-1
https://doi.org/10.1016/s0040-4020(99)00857-1
Autor:
József Fetter, György M. Keser″u, T. Czuppon, Le Thanh Giang, Gábor Czira, Károly Lempert, Ferenc Bertha, Mária Kajtár-Peredy
Publikováno v:
Tetrahedron. 55:8457-8474
The tetrazolyl groups of azetidin-2-ones 1a-e and 1h interfere with the normal reaction of related azetidin-2-ones with lead(IV) acetate, viz. acetoxylation at C-4, and cause formation of tetracyclic products 3a-e and 3h. Similar reactions take place
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a0df2f730d4bae8d6150a8e5c630a7d
https://doi.org/10.1016/s0040-4020(99)00432-9
https://doi.org/10.1016/s0040-4020(99)00432-9
Publikováno v:
Tetrahedron. 52:10169-10184
Treatment of pyrrolidinone 3a with CAN under the usual conditions leads to formation of spiro compound 12, rather than to N-demethoxyphenylation. A study of the reactions of compound 12 with sodium chloride and sodium iodide furnished the proof for o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daa0a684bd536543a3357cd9ded10f6f
https://doi.org/10.1016/0040-4020(96)00539-x
https://doi.org/10.1016/0040-4020(96)00539-x
Publikováno v:
Tetrahedron. 50:4185-4200
1-(4-methoxyphenyl)azetidin-2-ones 12 and 13, when treated with cerium(IV) ammonium nitrate (CAN), afford either their N-deprotected derivatives (19, 26) or the chlorinated compounds 22 and 27, respectively, as the main products, depending on whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f6ccee59f5cfb5422b6c01ffd3b7abc
https://doi.org/10.1016/s0040-4020(01)86713-2
https://doi.org/10.1016/s0040-4020(01)86713-2
Publikováno v:
ChemInform. 25
1-(4-methoxyphenyl)azetidin-2-ones 12 and 13, when treated with cerium(IV) ammonium nitrate (CAN), afford either their N-deprotected derivatives (19, 26) or the chlorinated compounds 22 and 27, respectively, as the main products, depending on whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53d50b115f283ab1309560aea3406fe6
https://doi.org/10.1002/chin.199433147
https://doi.org/10.1002/chin.199433147