204512-95-8Relevant articles and documents
Expeditious novel routes to enantiopure 3-amino tetrahydrofuran hydrochloride
Ramanujam, Rajendran,Ganjihal, Savita,Kalyanam, Nagabushanam,Majeed, Muhammed
, p. 663 - 668 (2013/07/11)
The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l-aspartic acid or l-methionine is described. The process involves no chromatography and can be easily carried out on a large scale. The enantiopurity of the final product was established by NMR and chiral HPLC methods.
N6 mono heterocyclic substituted adenosine derivatives
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, (2008/06/13)
A substituted N 6 -oxa, thia, thioxa and azacycloalkyl substituted adenosine derivative and a method for using the composition as an A 1 heart adenosine receptor.