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- 英文名：
31-Oxo-13-tert-Butyldimethylsilyloxyethyl Everolimus
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
N/A
31-Oxo-13-tert-Butyldimethylsilyloxyethyl Everolimus
N/A
C60H95NO14
1054.39
No Data Available
No Data Available
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文献和实验31-Oxo-13-tert-Butyldimethylsilyloxyethyl Everolimus
N/A
C60H95NO14
1054.39
No Data Available
No Data Available
, the ultraviolet (UV) (9 –12 ), and the postcolumn UV derivatization with 4,4′-dithiopyridine (13 ) and 5,5-dithiobis (2-nitrobenzoic acid) (14 ), the precolumn fluorescence derivatization with 4-(aminosulfonyl)- or ammonium-7-fluoro-2,1,3-benzoxadiazole
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
a solid?phase approach are presented. Curr. Protoc. Nucleic Acid Chem. 43:15.4.1?15.4.13. © 2010 by John Wiley & Sons, Inc. Keywords: (S)?HPMPC; (S)?HPMPA; peptidomimetic prodrugs; acyclic nucleoside phosphonates
?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
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