35760-86-2(35760-86-2)名称与标识符
35760-86-2(35760-86-2)相关文献
- 1. Synthesis of 7-alkynylated 8-aza-7-deaza-2′-deoxyadenosines via the Pd-catalysed cross-coupling reaction
Frank Seela,Matthias Zulauf J. Chem. Soc. Perkin Trans. 1 1998 3233 - 2. Oligonucleotides incorporating 8-aza-7-deazapurines: synthesis and base pairing of nucleosides with nitrogen-8 as a glycosylation position
Junlin He,Frank Seela Org. Biomol. Chem. 2003 1 1873 - 3. 6-Azauracil or 8-aza-7-deazaadenine nucleosides and oligonucleotides: the effect of 2′-fluoro substituents and nucleobase nitrogens on conformation and base pairing
Frank Seela,Padmaja Chittepu Org. Biomol. Chem. 2008 6 596 - 4. Vilsmeier reagent-mediated synthesis of 6-[(formyloxy)methyl]-pyrazolopyrimidines via a one-pot multiple tandem reaction
Shi-Han Lu,Po-Lin Liu,Fung Fuh Wong RSC Adv. 2015 5 47098 - 5. Vilsmeier reagent-mediated synthesis of 6-[(formyloxy)methyl]-pyrazolopyrimidines via a one-pot multiple tandem reaction
Shi-Han Lu,Po-Lin Liu,Fung Fuh Wong RSC Adv. 2015 5 47098 - 6. Synthesis and in vitro antiproliferative activity of novel pyrazolo[3,4-d]pyrimidine derivatives
Nermin S. Abdou,Rabah A. T. Serya,Ahmed Esmat,Mai F. Tolba,Nasser S. M. Ismail,Khaled A. M. Abouzid Med. Chem. Commun. 2015 6 1518 - 7. Design, synthesis, and biological evaluation with molecular dynamics study of novel pyrazolo[3,4-d]pyrimidine derivatives as anti-cancer agents
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Rania M. Shaban,Nermin Samir,Yassin M. Nissan,Khaled A. M. Abouzid RSC Adv. 2023 13 17074 - 9. Novel pyrazolo[3,4-d]pyrimidine derivatives: design, synthesis, anticancer evaluation, VEGFR-2 inhibition, and antiangiogenic activity
Ahmed M. Abdelhamed,Rasha A. Hassan,Hanan H. Kadry,Amira A. Helwa RSC Med. Chem. 2023 14 2640 - 10. 3,4-Diaminopyrazolo[3,4-d]pyrimidines: a new three-component microwave-assisted synthesis and anti-leukemic properties
Jia Hui Ng,Felicia Phei Lin Lim,Edward R. T. Tiekink,Anton V. Dolzhenko Org. Biomol. Chem. 2023 21 3432
![3-[(2-tert-butyl-5-methoxy-1,3-benzothiazol-6-yl)carbamothioylsulfanyl]propanoic acid](http://hg.y866.cn/compound/lib/scimg/cas/150/81059-04-3.png "3-[(2-tert-butyl-5-methoxy-1,3-benzothiazol-6-yl)carbamothioylsulfanyl]propanoic acid")
![[(1aS,1bα,5aα,6aβ)-2α-(β-D-Glucopyranosyloxy)-1a,1b,2,5a,6,6a-hexahydro-1aβ-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-6α-yl]α-D-galactopyranoside](http://hg.y866.cn/compound/lib/scimg/cas/150/81720-06-1.png "[(1aS,1bα,5aα,6aβ)-2α-(β-D-Glucopyranosyloxy)-1a,1b,2,5a,6,6a-hexahydro-1aβ-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-6α-yl]α-D-galactopyranoside")
