65384-67-0Relevant articles and documents
Gold-catalyzed homo- And cross-annulation of alkynyl carboxylic acids: a facile access to substituted 4-hydroxy 2: H -pyrones and total synthesis of pseudopyronine A
Choudhary, Shivani,Gayyur,Ghosh, Nayan,Saxena, Anchal
, p. 8716 - 8723 (2020/11/17)
A Au(i)-catalyzed homo- and cross-annulation reaction of alkynyl carboxylic acids offering 3,6-disubstituted 4-hydroxy 2H-pyrones has been demonstrated. The reaction tolerates various substituted alkynyl carboxylic acids and moderate to good yields of α-pyrone scaffolds have been observed. Later, a gram-scale reaction of the acid and the total synthesis of the natural product pseudopyronine A have been carried out successfully.
Investigation of the interaction of 5-aryl-2,3-dihydro-2,3-furandiones with compounds containing C=N and C≡N bonds simultaneously
Nekrasov,Shurov
, p. 1245 - 1254 (2007/10/03)
Aroylketenes, generated by the thermolysis of 5-aryl-2,3-dihydro-2,3- furandiones, react with S-methyl-N-cyano-N′-phenylisothiourea, N-cyano-N′,N′-dimethylformamidine, and N,N-bis(β-cyanoethyl) cyanamide with the formation of 6-aryl-2-[(methylthio)(phenyl
REACTION OF 5-ARYL-2,3-DIHYDRO-2,3-FURANDIONES WITH ISOPROPOXYETHYLENE
Shurov, S. N.,Livantsova, L. I.,Pavlova, E. Yu.,Zaitseva, G. S.,Kolesnikova, O. N.,Andreichikov, Yu. S.
, p. 190 - 191 (2007/10/02)
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