Reactions of 4,4′-difluoro-biphenyl-3,3′-dicarboxylic acid dimethyl ester with amino alcohols. A convenient route to biphenyl tetra-alcohols

2001 ◽  
Vol 42 (9) ◽  
pp. 1603-1606 ◽  
Author(s):  
Zihong Guo ◽  
Arthur G Schultz
EFSA Journal ◽  
2017 ◽  
Vol 15 (5) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
Claudia Bolognesi ◽  
Jean‐Pierre Cravedi ◽  
Karl‐Heinz Engel ◽  
...  

1981 ◽  
Vol 36 (8) ◽  
pp. 1037-1046 ◽  
Author(s):  
A. Römer ◽  
H. Scholl ◽  
H. Budzikiewicz

Abstract The structure elucidation of several minor phenazine pigments of Pseudomonads is described. 4-Hydroxyphenazine-1,6-dicarboxylic acid dimethyl ester, 2,3-dihydroxyphenazine, 2,3,7-trihydroxyphenazine, 4-hydroxyphenazine-1-carboxylic acid, 2,3-dihydroxyphenazine-1-carboxylic acid, 2,6-dihydroxyphenazine-1-carboxylic acid and 2,3,7-trihydroxyphenazine-1,6-dicarboxylic acid are new phenazine derivatives. The distribution of phenazines in the genus Pseudomonas is investigated.


1977 ◽  
Vol 55 (6) ◽  
pp. 975-978 ◽  
Author(s):  
E. G. Lewars ◽  
G. Morrison

Flash thermolysis of dimethyl 3-oxatricyclo[3.2.2.02,4]nona-6,8-diene-6,7-dicarboxylate (the oxide of barrellene-2,3-dicarboxylic acid dimethyl ester) (2) at 700 °C gave methyl isocoumarin-7-carboxylate (3) as a major component of the thermolysate. The rearrangement is discussed in terms of sigmatropic shifts in cycloheptatrienes and their norcaradiene tautomers.


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