54023-01-7Relevant articles and documents
Derivatives of (R)-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific Activity
Zhao, Fabao,Atxabal, Unai,Mariottini, Sofia,Yi, Feng,Lotti, James S.,Rouzbeh, Nirvan,Liu, Na,Bunch, Lennart,Hansen, Kasper B.,Clausen, Rasmus P.
, p. 734 - 746 (2022/01/03)
NMDA receptors mediate glutamatergic neurotransmission and are therapeutic targets due to their involvement in a variety of psychiatric and neurological disorders. Here, we describe the design and synthesis of a series of (R)-3-(5-furanyl)carboxamido-2-am
An efficient synthesis of N,N-Dialkyl-5-(chlorophenyl)-2-furancarbothioamides from 2-furoic acid
Lee, Hee Ju,Lee, Jae In
, p. 457 - 461 (2016/12/14)
An efficient synthesis of N,N-dialkyl-5-(chlorophenyl)-2-furancarbothioamides from 2-furoic acid was performed under mild conditions as inhibitor candidates of plant growth. 5-(Chlorophenyl)-2-furoic acids (3a-d) were prepared by treating 2-furoic acid wi
Synthesis of some thiadiazolotriazinone derivatives as possible antimicrobial agents
Prasad, D. Jagadeesh,Karthikeyan,Karegoudar, Prakash B.,Poojary, Boja,Holla, B. Shivarama,Kumari, N. Suchetha
, p. 1083 - 1091 (2008/02/01)
A series of 7-substituted-3-t-butyl 4(H)-1,3,4-thiadiazolo(2,3-c)-1,2,4- triazine-4-one (3) have been synthesized by condensing 4-amino-6-t-butyl-3- mercapto-1,2,4-triazin-5(4H)-one (1) with substituted Arylfuroic acids (2) using POCl3 as a cyclizing agen