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pro vyhledávání: '"Meda Haritha"'
Autor:
Manam Sreenivasa Rao, Meda Haritha, N. Chandrasekhar, Mandava V. Basaveswara Rao, Manojit Pal
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2697-2703 (2019)
Designed as potential cytotoxic agents a series of 6-substituted 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinoline derivatives were synthesized by using a Bischler type reaction. The methodology involved the cyclodehydration of 2-(3,4-dihydroquinolin-1(2H)-y
Externí odkaz:
https://doaj.org/article/eafc3eeef1bf481b844a61f4a1864b9a
Publikováno v:
Letters in Drug Design & Discovery. 15:160-168
Background: We report the design, synthesis and evaluation of a series of 4-biaryl substituted 2-amino benzo[h]chromene derivatives as potential cytotoxic agents. Methods: The one-pot synthesis of this class of compounds was carried out under ultraso
Autor:
Manojit Pal, Mandava Venkata Basaveswara Rao, Manam Sreenivasa Rao, Meda Haritha, N. Chandrasekhar
Publikováno v:
Tetrahedron Letters. 55:1660-1663
A greener and practical synthesis of 5-substituted thieno[2,3- c ]pyran-7-ones has been achieved via Cu-catalyzed coupling-cyclization of 3-iodothiophene-2-carboxylic acid with terminal alkynes in the presence of K 2 CO 3 in PEG 400 under ultrasound
Publikováno v:
ChemInform. 45
The title compounds (III) are obtained via a two-step one-pot synthesis involving the construction of the cyclohexanone ring from aromatic aldehydes and β-ketoesters as initial step under mild reaction conditions.
Autor:
N. Chandrasekhar, Mandava Venkata Basaveswara Rao, Meda Haritha, Manam Sreenivasa Rao, Manojit Pal
Publikováno v:
ChemInform. 45
A reaction mechanism for this inexpensive and easy thienopyranone synthesis is also proposed.
The 4,5,6,7-tetrahydro-1H-indazol-3(2H)-one derivatives have been synthesized in good yields via a two-step method in a single pot. The initial step involved the construction of cyclohexanone ring from aromatic aldehydes and β-ketoester in i-PrOH us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9667ce542b4ef518e9e5fefd66c2763