27285-14-9Relevant articles and documents
Synthesis of some triazolothienopyrimidin-5(4H)-ones
Pathak, U S,Gandhi, N V,Singh, S,Warde, R P,Jain, K S
, p. 223 - 229 (2007/10/02)
A series of hitherto unreported 1-(un)substituted-4-phenyltriazolothienopyrimidin-5(4H)-ones (8a-k) have been synthesized by the condensation of 2-hydrazino-3-phenylthienopyrimidin-4(3H)-ones (7a,b) with various one-carbon dono
METHYL N-ARYLDITHIOCARBAMATES: USEFUL REAGENTS FOR THE ANNELATION OF PYRIMIDINES AND 1,3-OXAZINES TO FIVE-MEMBERED HETEROCYCLIC RINGS
Garin, Javier,Loscertales, Maria Pilar,Melendez, Enrique,Merchan, Francisco L.,Rodriguez, Ricardo,Tejero, Tomas
, p. 1303 - 1312 (2007/10/02)
The reaction of methyl N-aryldithiocarbamates with ?-excessive heteroaromatic o-amino acid derivatives leads to the annelation of 4-oxo-2-thioxopyrimidines, 2,4-dioxopyrimidines or 2-arylamino-1,3-oxazines, depending on the reaction conditions.
Studies on Fused-ring Mesoionic Thiazolothienopyrimidine Systems
Talukdar, P. D.,Sengupta, S. K.,Datta, A. K.
, p. 538 - 542 (2007/10/02)
Cyclodehydration of 2-carboxymethylmercaptothienopyrimidin-4(3H)-ones (IV) have been studied.IV (R3=R4=Ph and R3=Me,R4=Ph) on reaction with acetic anhydride and pyridine mixture readily yield stable fusedring mesoionic systems (VI).While IV (R3=Ph,