One-pot facile conversion of Baylis-Hillman adducts into 1,5-diarylpyrazoles using microwave irradiation
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[1] M. Mamaghani,et al. AN EASY CONVERSION OF THE BAYLIS-HILLMAN ADDUCTS INTO tert-BUTYLDIMETHYLSILYL ETHERS WITH tert-BUTYLDIMETHYLSILYL CHLORIDE AND Li2S , 2004 .
[2] N. Haddad,et al. Application of the Palladium-Catalyzed N-Arylation of Hydrazones to Deactivated Heteroaryl Halides in the Synthesis of Pyrazoles. , 2004 .
[3] S. Swaney,et al. Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant: lead identification and SAR of 3- and 4-substituted derivatives. , 2000, Journal of medicinal chemistry.
[4] M. Kurth,et al. Fused pyrazolo heterocycles: intramolecular [3+2]-nitrile oxide cycloadditions applied to syntheses of pyrazolo [3,4-g] [2,1] dihydrobenzoisoxazol (in) es , 1999 .
[5] G. Marazzi,et al. A General, [1 + 4] Approach to the Synthesis of 3(5)-Substituted Pyrazoles from Aldehydes. , 1998 .
[6] G. Fabrizi,et al. Functionalised Pyrazoles through a Facile One-Pot Procedure from N-Tosyl-N-propargyl-hydrazine and Aryl Iodides or Vinyl Triflates , 1997 .
[7] J. Lyga,et al. Synthesis, mechanism of action, and QSAR of herbicidal 3‐substituted‐2‐aryl‐4,5,6,7‐tetrahydroindazoles , 1994 .
[8] Synlett , 2022 .