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942-58-5
Allyl O-Cumenyl Ether
942-58-5
C₁₂H₁₆O
176.25
Clear Colourless Oil
DCM, Ethyl Acetates, Hexanes
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文献和实验Allyl O-Cumenyl Ether
942-58-5
C₁₂H₁₆O
176.25
Clear Colourless Oil
DCM, Ethyl Acetates, Hexanes
of RT Master Mix to each sample. 4. Incubate 42ºC, 2 hrs. B. RNA Hydrolysis 1. To each sample add: 12.5 1N NaOH 5 µL 0.5 M EDTA 2. Incubate at 65ºC, 15 min. 3. Neutralize each sample with: 20 µL 2M HEPES O
Synthesis of 2-O-Alkyloligoribonucleotides
2′-O -Alkyloligoribonucleotides possess properties that render them ideally suited for studying RNA processing and for the affinity chromatography of RNA-protein complexes. Particularly useful compounds are those in which alkyl is methyl (1 –
Synthesis of Dipeptides with [CH20] Amide Bond Mimetics
This chapter describes the synthetic procedures leading to ether dipeptide isosteres of the Phe-ψ[CH 2 O]-spiro-C x ( 9a–9e , Fig. 1 ) and Phe-ψ[CH 2 O]-Allylglycine ( 13 , Fig. 2 ). Development of methods which lead to mimetics of amide
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