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909567-52-8
N,N’-Bis[(S)-1-(tert-Butyldimethylsilyloxymethyl)propyl]ethanediamide
909567-52-8
C₂₂H₄₈N₂O₄Si₂
460.8
Pale Yellow Solid
Chloroform, Dichloromethane, DMSO, Methanol
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文献和实验N,N’-Bis[(S)-1-(tert-Butyldimethylsilyloxymethyl)propyl]ethanediamide
909567-52-8
C₂₂H₄₈N₂O₄Si₂
460.8
Pale Yellow Solid
Chloroform, Dichloromethane, DMSO, Methanol
. GC-MS methods based on the conversion into tert -butyldimethylsilyl (33 ) and N(O,S)-propoxycarbonyl propyl ester (34 ) derivatives, and LC-MS method were highly sensitive and specific, but these methods require expensive equipment. Furthermore, CZE
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
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
‐Ethyldiisopropylamine, (DIEA; Alfa Aesar), freshly distilled over KOH Amino acids or dipeptide: Methyl N ‐(tert ‐butoxycarbonyl
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