N-[[P(S),2′R]-2′-Deoxy-2′-fluo
ro-2′-methyl-P-phenyl-5′-uridylyl]-L-alanine Methyl Ester- 询价
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- 2025年07月12日
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- 英文名：
N-[[P(S),2′R]-2′-Deoxy-2′-fluoro-2′-methyl-P-phenyl-5′-uridylyl]-L-alanine Methyl Ester
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
1394157-34-6
N-[[P(S),2′R]-2′-Deoxy-2′-fluoro-2′-methyl-P-phenyl-5′-uridylyl]-L-alanine Methyl Ester
1394157-34-6
C20H25FN3O9P
501.4
No Data Available
No Data Available
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文献和实验N-[[P(S),2′R]-2′-Deoxy-2′-fluoro-2′-methyl-P-phenyl-5′-uridylyl]-L-alanine Methyl Ester
1394157-34-6
C20H25FN3O9P
501.4
No Data Available
No Data Available
Preparation of 2′‐Deoxy‐2′‐Methylseleno‐Modified Phosphoramidites and RNA
1.15.2 Preparation of a 2′‐deoxy‐2′‐methylselenocytidine phosphoramidite building block for RNA solid‐phase synthesis (see ). DMAP, 4‐( N , N ‐dimethylamino)pyridine; DMF, N , N ‐dimethylformamide; DMTr, 4,4′‐dimethoxytrityl; TBAF, tetra‐ n
of 7‐bromo‐7‐deaza‐2′‐deoxyisoguanosine (S.4c ) is carried out by glycosylation of a brominated nucleobase followed by amination at C4 and selective deamination at C2′. NBS, N ‐bromosuccinimide; Piv, pivaloyl; TDA‐1, tris[2‐(2‐methoxyethoxy)ethyl]amine
Synthesis of Building Blocks and Oligonucleotides with {G}O6‐Alkyl‐O6{G} Cross‐Links
Basic Protocol 3: Synthesis of 1‐{O6‐[3′‐O‐tert‐Butyldimethysilyl‐5′‐O‐Dimethoxytrityl‐N2‐Phenoxyacetyl‐2′‐Deoxyguanidyl]}‐7‐{O6‐[5′‐O‐Dimethoxytrityl‐N2‐Phenoxyacetyl‐2′‐Deoxyguanidyl‐3′‐O‐(β‐2‐Cyanoethyl‐N,N′‐Diisopropyl)Phosphoramidite]}‐Heptane
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