Synthesis of .beta.-Dicarbonyl Compounds via the Conjugate Addition of Benzaldoximate Anion to .alpha.,.beta.-Acetylenic Carbonyl Compounds

1994 ◽  
Vol 59 (5) ◽  
pp. 1219-1221 ◽  
Author(s):  
Virginia Gomez ◽  
Arturo Perez-Medrano ◽  
Joseph M. Muchowski
Synthesis ◽  
2019 ◽  
Vol 51 (17) ◽  
pp. 3259-3268
Author(s):  
Xia Jiang ◽  
Hui Jin ◽  
Tingshu Wang ◽  
Hyebin Yoo ◽  
Sangho Koo

Efficient synthetic method for medicinally and opto-electronically important bichalcophenes is reported, which highlights Mn(OAc)3/CoCl2-catalyzed oxidative deacetylation of 1,5-dicarbonyl compounds that were easily prepared by conjugate addition of ethyl acetoacetate to α,β-unsaturated carbonyl compounds containing a chalcophene unit. Paal–Knorr reaction of the resulting 1,4-dicarbonyl compounds produced 4-phenyl-2,2′-bichalcophenes and their aza-analogues.


1977 ◽  
Vol 16 (12) ◽  
pp. 3059-3063 ◽  
Author(s):  
Charles P. Casey ◽  
William R. Brunsvold ◽  
Daniel M. Scheck

1987 ◽  
Vol 35 (2) ◽  
pp. 570-577 ◽  
Author(s):  
YASUMITSU TAMURA ◽  
TAKAYUKI YAKURA ◽  
HIROAKI TERASHI ◽  
JUN-ICHI HARUTA ◽  
YASUYUKI KITA

1994 ◽  
Vol 59 (12) ◽  
pp. 3500-3502 ◽  
Author(s):  
Masakazu Yamashita ◽  
Yoshifumi Tanaka ◽  
Akishi Arita ◽  
Minoru Nishida

1997 ◽  
Vol 38 (42) ◽  
pp. 7313-7316 ◽  
Author(s):  
Bonnie L. MacLean ◽  
Kimberlea A. Hennigar ◽  
Kevin W. Kells ◽  
Robert D. Singer

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