22325-27-5Relevant articles and documents
2-substituted benzylthio-5-(4,6-dimethyl pyrimidine-2-)thiomethyl-1,3,4-oxadiazole compound and application thereof
-
Paragraph 0024, (2016/10/10)
The invention relates to a 2-substituted benzylthio-5-(4,6-dimethyl pyrimidine-2-)thiomethyl-1,3,4-oxadiazole compound and an application thereof. The compound provided by the invention is easy to prepare, and the aftertreatment is convenient; and the obtained compound is used as a bactericide against gotryis cinerea, fusarium oxysporum, fungus colletorichum acutatum, strawberry anthracnose or colletotrichum gloeosporioides and shows relatively good bacteriostatic activity.
2-substituted benzylthio-5-(4,6-dimethyl pyrimidine-2-)sulfur methyl-1,3,4-thiadiazole compound and application thereof
-
Paragraph 0022, (2016/10/17)
The invention relates to a 2-substituted benzylthio-5-(4,6-dimethyl pyrimidine-2-)sulfur methyl-1,3,4-thiadiazole compound and application thereof. The compound is simple in preparation method, after-treatment is convenient, and the obtained compound has obvious effects when applied as bactericide for botryis cinerea, fusarium oxysporum, fungus colletorichum acutatum, strawberry anthracnose and colletotrichum gloeosporioides.
Carboxyl activation of 2-mercapto-4,6-dimethylpyrimidine through n-acyl-4,6-dimethylpyrimidine-2-thione: A chemical and spectrophotometric investigation
Rajan
, p. 287 - 291 (2015/01/30)
2-Mercapto-4,6-dimethylpyrimidine, as effective carboxyl activating group, has been successfully proved by converting it into respective acyl derivatives and the subsequent conversion to the amides and esters respectively using amines, amino alcohols and alcohols. The aminolysis and esterification were monitored chemically and spectrophotometrically. This paved way to establish that the above mercaptopyrimidine derivative is an efficient carboxyl activating group applicable in solid phase peptide synthesis.