A novel synthetic approach to 4-acetamido-1-arylindazoles via Semmler–Wolff rearrangement of 1-aryl-6, 7-dihydro-5H-indazol-4-one oxime
…, A Murugan, S Ramasubramanian, P Ramachandra…
Index: Manjunatha, Sulur G.; Bachu, Sreekanth; Kadambar, Vasantha Krishna; Murugan, Andiappan; Ramasubramanian, Sridharan; Ramachandra, Puranik; Nambiar, Sudhir Tetrahedron Letters, 2014 , vol. 55, # 22 p. 3348 - 3350
Full Text: HTML
Citation Number: 1
Abstract
The major limitations of the above synthetic methods are that these require 1,2,3-suitably substituted aromatic compounds such as 1 and 3, as the starting materials. Moreover, these procedures involve energetic intermediates and starting materials which may pose significant challenge for the scale up. Recently, a few notable methods are reported for the syntheses of 4-aminoindazoles via Buchwald amination of 4-haloindazoles. 5 We believe that there is a need for the ...
Related Articles:
Catalyst-free one-pot synthesis of 1, 4, 5-trisubstituted pyrazoles in 2, 2, 2-trifluoroethanol
[Alinezhad, Heshmatollah; Tajbakhsh, Mahmood; Zare, Mahboobeh Journal of Fluorine Chemistry, 2011 , vol. 132, # 11 p. 995 - 1000]
Aqueous one-pot synthesis of pyrazoles, pyrimidines and isoxazoles promoted by microwave irradiation
[Molteni, Valentina; Hamilton, Matthew M.; Mao, Long; Crane, Christine M.; Termin, Andreas P.; Wilson, Dean M. Synthesis, 2002 , # 12 p. 1669 - 1674]