α, α??Dibromoketones: A Superior Alternative to α??Bromoketones in Hantzsch Thiazole Synthesis
R Prakash, A Kumar, R Aggarwal…
Index: Prakash, Richa; Kumar, Ajay; Aggarwal, Ranjana; Prakash, Om; Singh Synthetic Communications, 2007 , vol. 37, # 15 p. 2501 - 2505
Full Text: HTML
Citation Number: 27
Abstract
Abstract α, α??Dibromoketones (2) have been found to be a superior alternative to the conventionally used α??bromoketones (1) for performing the Hantzsch thiazole synthesis. 1 These crystalline, nonlachrymatory compounds are more reactive than 1 as demonstrated by their reaction with 3, 5??dimethyl??1??thiocarboxamide (5).
Related Articles:
[Aggarwal, Ranjana; Kumar, Sunil; Singh, Shiv P. Journal of Sulfur Chemistry, 2012 , vol. 33, # 5 p. 521 - 525,5]
[Aggarwal, Ranjana; Kumar, Sunil; Singh, Shiv P. Journal of Sulfur Chemistry, 2012 , vol. 33, # 5 p. 521 - 525,5]
A facile one-pot synthesis of 2-pyrazolyl-4-aryl-thiazoles in a three-component reaction
[Nalajam, Guravaiah; Vedula, Rajeswar Rao Journal of Chemical Research, 2008 , # 4 p. 195 - 197]
1-heterylpyrazoles and their radioprotective properties
[Novikova, A. P.; Postovskii, I. Ya.; Puchkova, S. M.; Chechulina, L. A.; Tuzhilkova, T. N. Pharmaceutical Chemistry Journal, 1980 , vol. 14, # 6 p. 383 - 386 Khimiko-Farmatsevticheskii Zhurnal, 1980 , vol. 14, # 6 p. 46 - 49]