Selective catalytic addition of hydrogen halide and carboxylic acids and phenols to methyl esters of 1-alkyl-3-cyclopropenecarboxylic acids

Author(s):  
E. A. Shapiro ◽  
M. N. Protopopova ◽  
O. M. Nefedov

Author(s):  
M. N. Protopopova ◽  
E. A. Shapiro ◽  
Yu. V. Tomilov ◽  
I. E. Dolgii ◽  
O. M. Nefedov


2021 ◽  
pp. 174751982098715
Author(s):  
Khethobole C Sekgota ◽  
Michelle Isaacs ◽  
Heinrich C Hoppe ◽  
Ronnett Seldon ◽  
Digby F Warner ◽  
...  

Propylphosphonic acid anhydride has been successfully used as a coupling agent in the synthesis of a series of indolizine-2-carboxamido derivatives from indolizine-2-carboxylic acid and its 3-acetylated analogue. The acid substrates were obtained by saponification of the corresponding methyl esters produced, in turn, selectively and efficiently, by time-controlled cyclisation of a single Morita–Baylis–Hillman adduct. Various amino and hydrazino compounds with medicinal potential have been used to prepare indolizine-2-carboxamido and hydrazido derivatives.



ChemInform ◽  
2010 ◽  
Vol 41 (29) ◽  
pp. no-no
Author(s):  
V. A. Gorpinchenko ◽  
D. V. Petrov ◽  
S. S. Lozhkin ◽  
E. G. Galkin ◽  
V. A. Dokichev


ChemInform ◽  
2008 ◽  
Vol 39 (10) ◽  
Author(s):  
V. L. Gein ◽  
L. F. Gein ◽  
E. P. Tsyplyakova ◽  
O. S. Panova


2007 ◽  
Vol 43 (9) ◽  
pp. 1382-1386 ◽  
Author(s):  
V. L. Gein ◽  
L. F. Gein ◽  
E. P. Tsyplyakova ◽  
O. S. Panova




1985 ◽  
Vol 63 (9) ◽  
pp. 2522-2528 ◽  
Author(s):  
A. Kharrat ◽  
C. Gardrat ◽  
B. Maillard

The thermolysis of tert-butylperpent-4-enoate in various solvents ZH (carboxylic acids, anhydrides, methyl esters, nitriles) led to γ-butyrolactones 4-substituted by the group ZCH2 with good yields. The acidic treatment of the lactones 4 and 6 derived from non-functionalized alkanoic acids and methyl esters gave respectively the isomerized lactones 5 and 7, increasing the synthetic interest of the studied homolytic reaction.



1982 ◽  
Vol 13 (19) ◽  
Author(s):  
E. A. SHAPIRO ◽  
G. V. LUN'KOVA ◽  
A. O. NEFEDOV ◽  
I. E. DOLGII ◽  
O. M. NEFEDOV


Sign in / Sign up

Export Citation Format

Share Document