Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Satheeshvarma, Vanaparthi"'
Autor:
Faheem, Rosa M. Reguera, Banoth Karan Kumar, Estela Melcon-Fernandez, Nandikolla Adinarayana, Rafael Balana Fouce, Kondapalli Venkata Gowri Chandra Sekhar, Satheeshvarma Vanaparthi, Yolanda Perez-Pertejo Yolanda, Sankaranarayan Murugesan
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 40:12592-12607
Leishmaniasis is one of today's most neglected diseases. The emergence of new anti-leishmanial therapies emphasizes several study groups funded by the World Health Organization. The present investigation will focus on the research to determine a few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8501c6bf1bc7797383df3b83d9cda3c1
https://doi.org/10.1080/07391102.2021.1973564
https://doi.org/10.1080/07391102.2021.1973564
Autor:
Sravendra Rana, Amol Prakash Pawar, Satheeshvarma Vanaparthi, Mamta Mamta, Indresh Kumar, Eldhose Iype, Jyothi Yadav
Publikováno v:
Organic & Biomolecular Chemistry. 19:10601-10610
A two-pot synthesis of 5-aza-indoles has been developed from aqueous succinaldehyde and N-aryl propargylic-imines. This overall protocol involves (i) metal-free [3+2] annulation between aqueous succinaldehyde and N-aryl propargylic-imines to access 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd888278451797ea0018f7780716aca4
https://doi.org/10.1039/d1ob01949j
https://doi.org/10.1039/d1ob01949j
Autor:
Satheeshvarma, Vanaparthi, Mamta, Jyothi, Yadav, Amol Prakash, Pawar, Eldhose, Iype, Sravendra, Rana, Indresh, Kumar
Publikováno v:
Organicbiomolecular chemistry. 19(48)
A two-pot synthesis of 5-aza-indoles has been developed from aqueous succinaldehyde and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b11e5f44f0231f936e6083b2d0248ef
https://pubmed.ncbi.nlm.nih.gov/34859806
https://pubmed.ncbi.nlm.nih.gov/34859806
Autor:
Satheeshvarma Vanaparthi, Rajpal Singh, Nisar A. Mir, Sachin Choudhary, Panduga Ramaraju, Rajnish Prakash Singh, Preetika Sharma, Indresh Kumar, Murugesan Sankaranarayanan, Rajni Kant
Publikováno v:
New Journal of Chemistry. 44:16329-16339
A sequential multicomponent synthesis of highly substituted pyrrole-3-carboxaldehydes has been developed under metal-free conditions. This one-pot protocol involves proline-catalyzed direct chemoselective Mannich reaction-cyclization between 1,4-keto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fb0ab9685fe8010c3efc0e62aba4f79
https://doi.org/10.1039/d0nj03575k
https://doi.org/10.1039/d0nj03575k
Publikováno v:
RSC Advances. 9:24050-24056
An efficient protocol for the synthesis of 2,2-disubstituted indolin-3-ones under mild conditions has been developed. This reaction involves the copper-catalyzed in situ oxidative de-aromatization of 2-arylindoles to indol-3-one, followed by self-dim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beda10425575b051c44af617b313303f
https://doi.org/10.1039/c9ra04741g
https://doi.org/10.1039/c9ra04741g
Autor:
Nisar A. Mir, Jyothi Yadav, Sachin Choudhary, Amol Prakash Pawar, Rajni Kant, Ratika Sharma, Eldhose Iype, Satheeshvarma Vanaparthi, Mamta, Indresh Kumar
Publikováno v:
Organicbiomolecular chemistry. 18(6)
A simple and straightforward method for the synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes is developed from a common set of starting materials by tuning the reaction conditions. This sequential multicomponent protocol involves I2-mediated r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1d19dd8ca7e093dbade84115f9514bb
https://pubmed.ncbi.nlm.nih.gov/31976504
https://pubmed.ncbi.nlm.nih.gov/31976504
Publikováno v:
RSC advances. 9(42)
An efficient protocol for the synthesis of 2,2-disubstituted indolin-3-ones under mild conditions has been developed. This reaction involves the copper-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4cbf7919e1d2d814d68b4aa5004c37ab
https://pubmed.ncbi.nlm.nih.gov/35527913
https://pubmed.ncbi.nlm.nih.gov/35527913
Autor:
Satheeshvarma Vanaparthi, Nishant Jain, Lingaiah Nagarapu, Sridhara Janardhan, Rajashaker Bantu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 30:127304
A new series of 1,2,3-triazole tethered chalcone acetamide derivatives (7a-c & 8a-r) have been synthesized in excellent yields and their structures were determined by analytical and spectral (FT-IR, 1H NMR, 13C NMR & HRMS) studies. The newly synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::370f16862ed5b53668009f3216815296
https://doi.org/10.1016/j.bmcl.2020.127304
https://doi.org/10.1016/j.bmcl.2020.127304
Publikováno v:
ChemInform. 45
Two series of novel benzothiazolopyrimidine carboxamide derivatives (VI) and (VII) are synthesized and evaluated for their cytotoxicity against some human cancer cell lines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daeca0479520ffa77bb3d938f8ecd17d
https://doi.org/10.1002/chin.201415187
https://doi.org/10.1002/chin.201415187
Publikováno v:
European journal of medicinal chemistry. 69
A novel series of building blocks consisting of benzo[4,5]thiazolo[1,2- a ]pyrimidine-3-carboxylate have been synthesized as potential anticancer compounds. These compounds were prepared from 2-aminobenzothiazole, benzaldehyde and ethyl acetoacetate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7fed58fe8f2a4bcd154e1047275838
https://pubmed.ncbi.nlm.nih.gov/24113366
https://pubmed.ncbi.nlm.nih.gov/24113366