Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Honnappa, Nagarajaiah"'
Autor:
Avuthu, Vidya Sagar Reddy, Allaka, Tejeswara Rao, Patel, Pratik Rameshchandra, Venkatesan, Srinivasadesikan, Honnappa, Nagarajaiah, Afzal, Mohd, Kishore, Pilli Veera Venkata Nanda
Publikováno v:
In Journal of Molecular Structure 15 October 2024 1314
Autor:
Mohan, Pooja, Kalidasan, Kavya, Mallapur, Srinivas, Ramaraghavulu, Rajavaram, Vishwa, Prashanth, Kandaiah, Sakthivel, Honnappa, Nagarajaiah
Publikováno v:
In Hybrid Advances December 2023 4
Autor:
Dilip Kamble Soumyashree, Dinesh Shrikant Reddy, Honnappa Nagarajaiah, Lohit Naik, Hemantkumar Mohanchand Savanur, Choradi Devendrappa Shilpa, Mayanna Sunitha Kumari, Hamzad Shanavaz, Basavaraj Padmashali
Publikováno v:
Archiv der Pharmazie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d8ca46eb4ab03904c3bfb8ccd32e4fd
https://doi.org/10.1002/ardp.202300106
https://doi.org/10.1002/ardp.202300106
Akademický článek
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Autor:
Alankriti Bajpai, Samik Jhulki, Tahsin J. Chow, Honnappa Nagarajaiah, Jarugu Narasimha Moorthy
Publikováno v:
New Journal of Chemistry. 41:4510-4517
Three unique λ-, χ- and ψ-shaped tri- and tetaarylanthracenes, i.e., ANT1–3, have been designed and synthesized by Suzuki coupling as a key reaction for application as emissive and host materials in OLEDs. The regioisomeric anthracenes ANT2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac414d73968d09bbf552647c2c0a7afc
https://doi.org/10.1039/c7nj00324b
https://doi.org/10.1039/c7nj00324b
Publikováno v:
Tetrahedron Letters. 57:5135-5149
Biginelli reaction involves acid-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) using easily-accessible starting materials, namely, aldehyde, active methylene compound and (thio)urea. DHPMs have stimulated resurgence of intere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4698174429bd0eea825c33507340a3c
https://doi.org/10.1016/j.tetlet.2016.09.047
https://doi.org/10.1016/j.tetlet.2016.09.047
Publikováno v:
Organic & Biomolecular Chemistry. 14:4129-4135
α-Chloroketones - obtained by the atom-economical chlorination of ketones with trichloroisocyanuric acid (TCCA) in the presence of p-TSA under ball-milling conditions - were set up for a sequential base-mediated condensation reaction with thiourea/t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b459345730e5b52a213150138b2f03a5
https://doi.org/10.1039/c6ob00351f
https://doi.org/10.1039/c6ob00351f
Publikováno v:
European Journal of Organic Chemistry. 2015:2733-2738
It is shown that both tribromoisocyanuric acid (TBCA) and trichloroisocyanuric acid (TCCA) are excellent reagents for direct halogenation of electron-rich aromatics under solvent-free, ball-milling conditions. The results are remarkable in light of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7485efb7d837fd4353eab9e3ed00e5bc
https://doi.org/10.1002/ejoc.201403463
https://doi.org/10.1002/ejoc.201403463
Autor:
Palani Natarajan, Jarugu Narasimha Moorthy, Manchugondanahalli S Krishna, Honnappa Nagarajaiah, Paloth Venugopalan
Publikováno v:
CrystEngComm. 17:5307-5314
Based on structural studies already available for the cocrystals of a sterically-rigidified tetraarylpyrene (TP) host substituted at the periphery by flexible methoxymethyl (MM) groups, i.e., TPMM, with aliphatic guests, formation of ternary or three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cc5309bbccbee23d9bd56023387cff4
https://doi.org/10.1039/c5ce00243e
https://doi.org/10.1039/c5ce00243e
Publikováno v:
ChemInform. 47
Biginelli reaction involves acid-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) using easily-accessible starting materials, namely, aldehyde, active methylene compound and (thio)urea. DHPMs have stimulated resurgence of intere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a72291b3bb3db717bbb561a87c5b25fa
https://doi.org/10.1002/chin.201651240
https://doi.org/10.1002/chin.201651240