316352-59-7

Upstream product

• 4330-20-5 N-3-benzoylthymine 
• 540-51-2 2-bromoethanol 
• 65-71-4 thymin 
• 98-88-4 benzoyl chloride 

Downstream Products

• 77268-27-0 (2S)-benzyloxycarbonylamino-5-(1-thyminyl)pentanoic acid 
• 316352-63-3 (2S,4S)-3-benzyloxycarbonyl-2-tert-butyl-4-[3-(3-benzoyl-1-thyminyl)propyl]oxazolidin-5-one 
• 316353-11-4 (2S)-benzyloxycarbonylamino-5-(3-benzoyl-1-thyminyl)pentanoic acid 
• 316352-64-4 (2S,4S)-3-benzyloxycarbonyl-2-tert-butyl-4-[3-(1-thyminyl)propyl]oxazolidin-5-one 
• 316352-61-1 3-benzoyl-1-(2-iodoethyl)thymine 

Relevant academic research and scientific papers

Two simple protocols for the preparation of diallylaminoethyl-substituted nucleic bases: A comparison

The syntheses of pyrimidine and purine nucleic bases substituted with diallylaminoethyl groups are reported following two different protocols. A comparison is made between the yield, expense, and difficulty of each route.

Synthesis by conjugate radical addition of new heterocyclic amino acids with nucleic acid bases in their side chains

N-(2-Iodoethyl) and N-(3-iodopropyl)pyrimidines and purines undergo stereoselective conjugate radical addition with an optically active oxazolidinone acceptor to give syn-adducts that can be converted into pyrimidine and purine amino acids.