Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Adivireddy Padmaja"'
Autor:
Chokkappagari Premakumari, Akkarapalli Muralikrishna, Adivireddy Padmaja, Venkatapuram Padmavathi, Sea Jin Park, Tack-Joong Kim, Guda Dinneswara Reddy
Publikováno v:
Arabian Journal of Chemistry, Vol 7, Iss 4, Pp 385-395 (2014)
A new class of amido sulfonamido methane linked bis heterocycles- bis-oxazoles, thiazoles and imidazoles were prepared and screened for antimicrobial and anticancer activities. The chloro substituted amido sulfonamido bisimidazole exhibited excellent
Externí odkaz:
https://doaj.org/article/387c3ac36bba4b48a4d67df6b62e7f06
Autor:
Venkatapuram Padmavathi, Boggu Jagan Mohan Reddy, Akula Baliah, Adivireddy Padmaja, Dandu Bhaskar Reddy
Publikováno v:
ARKIVOC, Vol 2005, Iss 14, Pp 1-13 (2005)
Externí odkaz:
https://doaj.org/article/9fb9eb6d77ed4711824adc227196ed83
Autor:
Donthamsetty V Sowmya, Kuppireddy Gari Divya, Daggupati Trinath, Chitrala Kumaraswamy Naidu, Yeguvapalli Suneetha, Adivireddy Padmaja, Venkatapuram Padmavathi
Publikováno v:
Polycyclic Aromatic Compounds. :1-27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a21eac48e697e3272bb039b0df40a034
https://doi.org/10.1080/10406638.2022.2092875
https://doi.org/10.1080/10406638.2022.2092875
Autor:
Adivireddy Padmaja, N. Hussain Basha, Venkatapuram Padmavathi, P. Siva Shanker, G. Dinneswara Reddy, K. Narendra Babu
Publikováno v:
Polycyclic Aromatic Compounds. 42:7321-7335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f22763b9c33abecd3e6e458e8b14102b
https://doi.org/10.1080/10406638.2021.1998153
https://doi.org/10.1080/10406638.2021.1998153
Autor:
Adivireddy Padmaja, Dinneswara Reddy Guda, Venkatapuram Padmavathi, Tamatam Rekha, N. Hussain Basha
Publikováno v:
Polycyclic Aromatic Compounds. 42:5398-5410
A variety of azolyl pyrimidinyl acetamides were prepared from azolyl glycinate and 4,6-diaryl/heteroarylpyrimidinyl-2-amines in the presence of DMAP under ultrasonication. Nitrophenyl, pyridinyl an...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0fb6bd0072fc01f0ed0623cfe19e7ee
https://doi.org/10.1080/10406638.2021.1936084
https://doi.org/10.1080/10406638.2021.1936084
Autor:
Tankam Rajeswari, Venkatapuram Padmavathi, Adivireddy Padmaja, Panga Siva Sankar, Kayathi Narendra Babu
A variety of thiophenylazolyl pyrrolylsulfamoyl acetamides were prepared by the reaction of azolylsulfamoyl acetate with pyrrolylamine in the presence of sodium methoxide in methanol under ultrasonication. Chloro, nitro and dinitro substituted thioph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0de7ad78a04d9b7aa8f2877e7b637a78
https://doi.org/10.21203/rs.3.rs-921900/v1
https://doi.org/10.21203/rs.3.rs-921900/v1
Akademický článek
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Autor:
Tamatam Rekha, Guda Dinneswara Reddy, Adivireddy Padmaja, Venkatapuram Padmavathi, Tankam Rajeswari
Publikováno v:
Journal of Heterocyclic Chemistry. 56:2449-2459
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bc4f8e51227b306196fa6a08d795da
https://doi.org/10.1002/jhet.3634
https://doi.org/10.1002/jhet.3634
Publikováno v:
Archiv der PharmazieREFERENCES. 354(8)
A library of bis(azolyl)sulfonamidoacetamides was prepared by the reaction of azolylsulfonylamines with azolylchloroacetamides in the presence of pyridine/4-(dimethylamino)pyridine (DMAP) under ultrasonication. The reaction proceeded well with DMAP,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573434f16c2fe31e4a0399177eaca14c
https://pubmed.ncbi.nlm.nih.gov/33977563
https://pubmed.ncbi.nlm.nih.gov/33977563
Autor:
Guda Mallikarjuna Reddy, Cirandur Suresh Reddy, G. Sravya, Adivireddy Padmaja, Venkatapuram Padmavathi, Grigory V. Zyryanov, Nemallapudi Bakthavatchala Reddy, Jarem Raul Garcia, Avula Balakrishna
Publikováno v:
Journal of Heterocyclic Chemistry. 56:589-596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb118f628f6c6fa53934ac91cf781d22
https://doi.org/10.1002/jhet.3435
https://doi.org/10.1002/jhet.3435