Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Samikannu, Ramesh"'
Publikováno v:
Journal of the Iranian Chemical Society. 16:1197-1205
A remarkably simple synthetic method has been described for the access of structurally diverse 3,4-dihydropyrimidin-2(1H)-ones in excellent yields in the presence of 2,4,6-trichloro-1,3,5-triazine (TCT) as an efficient source of hydrochloric acid und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92a79323c7e735f3ee51ff60e6d4db57
https://doi.org/10.1007/s13738-019-01597-3
https://doi.org/10.1007/s13738-019-01597-3
Akademický článek
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Akademický článek
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Autor:
Poudel, Yam B., Rao, Chetana, Kotapati, Srikanth, Deshpande, Madhura, Thevanayagam, Lourdes, Pan, Chin, Cardarelli, Josephine, Chowdari, Naidu, Kaspady, Mahammed, Samikannu, Ramesh, Kuppusamy, Prakasam, Saravanakumar, Pon, Arunachalam, Pirama N., Deshpande, Shrikant, Rangan, Vangipuram, Rampulla, Richard, Mathur, Arvind, Vite, Gregory D., Gangwar, Sanjeev
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 January 2020 30(1)
Autor:
Samikannu Ramesh, Pon Saravanakumar, Arvind Mathur, Pirama Nayagam Arunachalam, Ramasamy Duraisamy
Publikováno v:
Journal of Chemical Sciences. 129:329-333
A facile and versatile method for the synthesis of alicyclic fused pyrimidones from aminoacrylates and lactams in the presence of phosphorous oxychloride is described. The results suggest that this method is widely applicable except for cyclobutyl fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eecd191c36b351f8e5f1e8b3d2d6203b
https://doi.org/10.1007/s12039-017-1244-z
https://doi.org/10.1007/s12039-017-1244-z
Autor:
Karmakar, Ananta, Nimje, Roshan Y., Silamkoti, Arundutt, Pitchai, Manivel, Basha, Mushkin, Singarayer, Christuraj, Ramasamy, Duraisamy, Babu, G. T. Venkatesh, Samikannu, Ramesh, Subramaniam, Srinath, Anjanappa, Prakash, Vetrichelvan, Muthalagu, Kumar, Hemantha, Dikundwar, Amol G., Gupta, Anuradha, Gupta, Arun Kumar, Rampulla, Richard, Dhar, T. G. Murali, Mathur, Arvind
Publikováno v:
Organic Process Research & Development; 4/16/2021, Vol. 25 Issue 4, p1001-1014, 14p
Autor:
Kulanthaivel Sivakumar, Appaswami Lalitha, Samikannu Ramesh, P. N. Arunachalam, Chiradeep Panja
Publikováno v:
Synthetic Communications. 40:3544-3551
The synthesis of α-aminonitriles by a direct three component Strecker reaction has been achieved in water, which is found to be an inexpensive, non-toxic and eco-friendly reaction medium for the nucleophilic addition. This protocol is effective to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::577cf7494192d3a78e1eac1f0dd97553
https://doi.org/10.1080/00397910903457381
https://doi.org/10.1080/00397910903457381
Publikováno v:
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry. 41:91-93
An efficient synthesis of 1,3-benzodioxoles was achieved from catechol with different aldehydes and ketones using Cu(II) impregnated sulfated MCM-41 as an efficient and reusable catalyst.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14d0f0fd16bad1d44ce97a2e990df36b
https://doi.org/10.1080/15533174.2010.538018
https://doi.org/10.1080/15533174.2010.538018
Autor:
Samikannu, Ramesh, Appaswami, Lalitha
Publikováno v:
Acta chimica Slovenica. 60(3)
A novel and practical method has been developed for the synthesis of β-cyanoketones using tetraethylammonium cyanide (Et4NCN, TEACN) / Sc(III) triflate and chalcones without the liberation of toxic HCN gas. Availability, safety, easy handling of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71bdaf42c06ccadf293bae12bd3396cb
https://pubmed.ncbi.nlm.nih.gov/24169725
https://pubmed.ncbi.nlm.nih.gov/24169725
Autor:
Samikannu Ramesh, Chiradeep Panja, P. N. Arunachalam, Kulanthaivel Sivakumar, Appaswami Lalitha
Publikováno v:
ChemInform. 42
α-Aminonitriles (IV) are formed exclusively and the methodology is compatible with various types of aldehydes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0a48338b3d228d2a708864407934b94
https://doi.org/10.1002/chin.201116075
https://doi.org/10.1002/chin.201116075