Derivatives of Furo[3,2-b]pyrrole

1994 ◽  
Vol 59 (2) ◽  
pp. 473-481 ◽  
Author(s):  
Alžbeta Krutošíková ◽  
Miloslava Dandárová ◽  
Vladimír Bobošík

A number of methyl 2-substituted, 2,3-disubstituted-4H-furo[3,2-b]pyrrole-5-carboxylates (V - VII) and methyl 1H-benzo[b]furo[3,2-b]pyrrole-2-carboxylate (VIII) was prepared by the thermolysis of corresponding methyl 2-azido-3-(R1,R2-substituted-2-furyl)propenoates (I - IV). N-Methyl and N-benzyl derivatives IX - XVI were prepared at the phase-transfer catalysis conditions. Hydrolysis of some N-methyl and N-benzyl substituted esters furnished corresponding acids XVII - XXII. The hydrazides XXIII - XXX were obtained from corresponding esters and hydrazine hydrate. The preparation of 1-benzylbenzo[b]furo[3,2-b]pyrrole (XXXI) is described as well.

2006 ◽  
Vol 39 (7) ◽  
pp. 2514-2520 ◽  
Author(s):  
Sergio A. Guillén-Castellanos ◽  
J. Scott Parent ◽  
Ralph A. Whitney

2014 ◽  
Vol 84 (8) ◽  
pp. 1641-1643 ◽  
Author(s):  
V. I. Rstakyan ◽  
A. E. Hakobyan ◽  
G. B. Zakaryan ◽  
S. S. Hayotsyan ◽  
H. S. Attaryan ◽  
...  

1984 ◽  
Vol 49 (8) ◽  
pp. 1780-1787 ◽  
Author(s):  
Štefan Kučár ◽  
Juraj Zámocký ◽  
Juraj Zemek ◽  
Dušan Anderle ◽  
Mária Matulová

Partial hydrolysis of per-O-acetyl- and per-O-benzoyl derivatives of 1,6-anhydro-β-D-glucopyranose with methanolic hydrogen chloride and hydrazine hydrate was investigated. The acyl group at C(3) is of substantial influence on the course of hydrolysis. The esterified hydroxyl group at C(3) was found to be most stable on acid hydrolysis with methanolic hydrogen chloride when compared with that at C(2), or C(4); on the other hand, this ester group is the most labile upon hydrolysis with hydrazine hydrate. Selectivity of the respective ester groups towards hydrolysis made it possible to prepare all variations of acetyl and benzoyl derivatives of 1,6-anhydro-β-D-glucopyranose.


1975 ◽  
Vol 30 (9-10) ◽  
pp. 825-826 ◽  
Author(s):  
Eckehard V. Dehmlow ◽  
Gordian C. Ezimora

Chloroform/concentrated aqueous NaOH/catalyst transform testosterone acetate (1) into a mixture of the α- and β-stereoisomers of dichlorocyclopropyl derivatives (2) and tetrachlorospiropentane derivates (3). 2 are the precursors of 3. Formation of analog chloro as well as bromo derivatives of cholestenone was demonstrated.


1988 ◽  
Vol 53 (4) ◽  
pp. 822-832 ◽  
Author(s):  
Jiří Svoboda ◽  
Zuzana Kocfeldová ◽  
Jaroslav Paleček

Under conditions of phase-transfer catalysis or in homogeneous solution of potassium tert-butoxide the title compounds give stereoisomeric mixtures of substituted 2,3-epoxy nitriles III and IV. Alkaline hydrolysis of epoxy nitriles IV afforded the corresponding 2-arylpropanals in low yields. On treatment with methanol and potassium carbonate, epoxy nitriles III and IV were converted into epoxy esters in good yields.


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