Zobrazeno 1 - 10
of 80
pro vyhledávání: '"apionucleosides"'
Autor:
Holan, Martin1 (AUTHOR) martin.holan@boehringer-ingelheim.com, Tucker, Kathryn1 (AUTHOR), Dyatkina, Natalia1 (AUTHOR), Liu, Hong1 (AUTHOR), Kinkade, April1 (AUTHOR), Wang, Guangyi1 (AUTHOR), Jin, Zhinan1 (AUTHOR), Prhavc, Marija1 (AUTHOR) mprhavc@its.jnj.com
Publikováno v:
Molecules. Apr2022, Vol. 27 Issue 8, pN.PAG-N.PAG. 17p.
Autor:
Martin Holan, Kathryn Tucker, Natalia Dyatkina, Hong Liu, April Kinkade, Guangyi Wang, Zhinan Jin, Marija Prhavc
Publikováno v:
Molecules, Vol 27, Iss 8, p 2413 (2022)
Nucleoside analogues have excellent records as anti-HBV drugs. Chronic infections require long-term administration ultimately leading to drug resistance. Therefore, the search for nucleosides with novel scaffolds is of high importance. Here we report
Externí odkaz:
https://doaj.org/article/52a1d42a2e4c43f7b5a961ce9ddce727
Autor:
Prhavc, Martin Holan, Kathryn Tucker, Natalia Dyatkina, Hong Liu, April Kinkade, Guangyi Wang, Zhinan Jin, Marija
Publikováno v:
Molecules; Volume 27; Issue 8; Pages: 2413
Nucleoside analogues have excellent records as anti-HBV drugs. Chronic infections require long-term administration ultimately leading to drug resistance. Therefore, the search for nucleosides with novel scaffolds is of high importance. Here we report
Autor:
Kim, Jihee, Hong, Joon Hee *
Publikováno v:
In Carbohydrate Research 2003 338(8):705-710
Autor:
Hong, Joon H., Gao, Mu-Yun, Choi, Yongseok, Cheng, Yung-Chi, Schinazi, Raymond F., Chu, Chung K. *
Publikováno v:
In Carbohydrate Research 2000 328(1):37-48
Publikováno v:
In Tetrahedron Letters 1999 40(2):231-234
Akademický článek
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Akademický článek
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Publikováno v:
Tetrahedron Letters. 40:231-234
Asymmetric synthesis of 3′- C -methyl-4′-thio apionucleosides was accomplished from the chiral intermediate 6 . The chirality of quaternary carbon of the key intermediate 6 was transferred from the chirality of secondary allylic alcohol 5 via [3,
Publikováno v:
ChemInform. 30
Asymmetric synthesis of 3′- C -methyl-4′-thio apionucleosides was accomplished from the chiral intermediate 6 . The chirality of quaternary carbon of the key intermediate 6 was transferred from the chirality of secondary allylic alcohol 5 via [3,