(4aS,11aR,12aS,13S)-3,7-bis(be
nzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-8-(dibenzylamino)-13-(dimethylamino)-10-fluoro-5-hydroxy-11a,12,12a,13-tetrahydrotetraceno[2,3-d]isoxazole-4,6(4aH,11H)-dione- 询价
- ITI Biochem
- 美国
- 1431558-60-9
- 2025年07月17日
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
(4aS,11aR,12aS,13S)-3,7-bis(benzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-8-(dibenzylamino)-13-(dimethylamino)-10-fluoro-5-hydroxy-11a,12,12a,13-tetrahydrotetraceno[2,3-d]isoxazole-4,6(4aH,11H)-dione
- 库存：
98
- 供应商：
北京孚博
- CAS号：
1431558-60-9
- 规格：
1g
CAS：1431558-60-9
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文献和实验Synthesis of Building Blocks and Oligonucleotides with {G}O6‐Alkyl‐O6{G} Cross‐Links
Introduction Basic Protocol 1: Protection of the Diol with a tert‐Butyldiphenyl Silyl Group Basic Protocol 2: Synthesis of O6‐2′‐Deoxyguanosine‐Alkyl‐O6‐2′‐Deoxyguanosine‐3′‐O‐bis‐Phosphoramidites
?isobutyryl?5??O ?(4,4??dimethoxytrityl)?2??O ?(propargyl)guanosine is converted to its 3??O ?levulinyl ester in a yield of 91%. The reaction of commercial N 2 ?isobutyryl?5??O ?(4,4??dimethoxytrityl)?2??O ?tert ?butyldimethylsilyl?3??O ?[(2?cyanoethyl)?N ,N
Materials 3′‐O ‐(tert ‐Butyldimethylsilyl)‐5′‐O ‐(4,4′‐dimethoxytrityl)‐thymidine (1 ; Wilds et al., )
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