Benghiat, Eric published the artcileSynthesis of S-3-indolemethyl derivatives of 5′-deoxy-5′-thioadenosine, Synthetic Route of 5654-92-2, the main research area is indolylmethylthiodeoxyadenosine; adenosine indolylmethylthiodeoxy.
The title compounds (I; R = H, Me) were prepared by reaction of the appropriate 3-indolemethyl thioacetate with 5′-deoxy-5′-chloroadenosine in basic media. 5′-Deoxy-5′-(3-indolemethylthio)adenosines unsubstituted at the indolic nitrogen, cannot be prepared via this route due to facile conversion of the precursor 3-indolemethylthiol derivative to the corresponding 3,3′-diindolemethyl sulfide.
Journal of Heterocyclic Chemistry published new progress about indolylmethylthiodeoxyadenosine; adenosine indolylmethylthiodeoxy. 5654-92-2 belongs to class indole-building-block, name is N,N-Dimethyl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)methanamine, and the molecular formula is C10H13N3, Synthetic Route of 5654-92-2.
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles