Use of N-acyl or N-alkyloxycarbonyl-aminotetrachlorophthalimides for the preparation of alkylhydrazines via the Mitsunobu protocol
MF Pinto, N Brosse, B Jamart-Grégoire
Index: Pinto, Maria-Fatima; Brosse, Nicolas; Jamart-Gregoire, Brigitte Synthetic Communications, 2002 , vol. 32, # 23 p. 3603 - 3610
Full Text: HTML
Citation Number: 11
Abstract
ABSTRACT N-acyl and N-alkyloxycarbonyl tetrachloro-aminophthalimides which are best acidic partners in the Mitsunobu reaction and more easily dephthaloylated than their unsubstituted analogs can be used efficiently for the preparation of 1, 1-substituted hydrazines.
Related Articles:
[Garcia, Jordi; Vilarrasa, Jaume Tetrahedron Letters, 1987 , vol. 28, # 3 p. 341 - 342]
[Brosse, Nicolas; Pinto, Maria-Fatima; Jamart-Gregoire, Brigitte Journal of Organic Chemistry, 2000 , vol. 65, # 14 p. 4370 - 4374]
[Klimova, Elena I.; Vazquez Lopez, Eduardo A.; Martinez Mendoza, Juan M.; Ramirez, Lena Ruiz; Alamo, Marcos Flores; Backinowsky, Leon V. Journal of Heterocyclic Chemistry, 2009 , vol. 46, # 3 p. 484 - 491]
[Klimova, Elena I.; Vazquez Lopez, Eduardo A.; Martinez Mendoza, Juan M.; Ramirez, Lena Ruiz; Alamo, Marcos Flores; Backinowsky, Leon V. Journal of Heterocyclic Chemistry, 2009 , vol. 46, # 3 p. 484 - 491]
[Garcia, Jordi; Vilarrasa, Jaume Tetrahedron Letters, 1987 , vol. 28, # 3 p. 341 - 342]