Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Amarnath Velidandi"'
Publikováno v:
Results in Chemistry, Vol 8, Iss , Pp 101560- (2024)
Newer Pyrrole-Chromones Chalcones (I–VII) were prepared by a simple method. among the series of compounds, compound −1 which was synthesized with 30 % of NaOH solution, at temperature of 60–65 °C with twelve hours of reaction time resulted in
Externí odkaz:
https://doaj.org/article/83c5ffd4e0094359bfe8888f67917dcd
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101425- (2024)
Existing of a cell depends on the pyrimidine moiety; it controls many functions which lead to alter the action of organs. Herein, we demonstrate the synthesis, biological evolution of newer pyrimidins. Titled compounds are formed with good yields, th
Externí odkaz:
https://doaj.org/article/85db7c531cce44a8bb60f084bdcc1ce9
Autor:
Madhavi Latha Duda, Amarnath Velidandi
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100697- (2023)
An efficient eco-friendly method, with less hazardous chemicals, developed for the deformylation and followed by halogenation of 3-formylchromones by applying easily available Oxone as oxidising agent and NaX as a halogenating source. Many of 3- halo
Externí odkaz:
https://doaj.org/article/b1058900cd5f4842b44163c2bc5f05cb
Autor:
Prasanna Bethanamudi, Srinivas Bandari, Kanakaraju Sankari, Amarnath Velidandi, G. V. P. Chandramouli
Publikováno v:
E-Journal of Chemistry, Vol 9, Iss 4, Pp 1676-1682 (2012)
The alkylation of 5-cyano indazoles 2 in the presence of readily available imidizolium salts (ionic liquids) (Bmim)BF4 as phase transfer catalyst were performed to afford the regio isomers N1-and N2-(substituted alkyl)-5-cyano indazoles. The N1-alkyl
Externí odkaz:
https://doaj.org/article/79a55302335d4221987d0b207026c617
Publikováno v:
Russian Journal of Bioorganic Chemistry. 49:76-80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9f41964c471de60ac0c1dc637e284a2
https://doi.org/10.1134/s1068162023010247
https://doi.org/10.1134/s1068162023010247
Publikováno v:
Russian Journal of Organic Chemistry. 58:1354-1357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27a1cc9110d194b44a88d897fa9f5fd6
https://doi.org/10.1134/s1070428022090238
https://doi.org/10.1134/s1070428022090238
Publikováno v:
Russian Journal of Organic Chemistry. 58:814-819
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a7f8e443bffe4bcf99e7120643d2b5f
https://doi.org/10.1134/s1070428022060094
https://doi.org/10.1134/s1070428022060094
Dihydro furan derivatives are potentially bioactive hence we started working on it prepared themfrom 2-(4-nitrophenyl)-2-oxoethyl 2-phenylacetate, reducing it and adding substituted carboxylic acids with EDCI, HOBt leads to the titled compounds. &nbs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6625191faf27969b4048946214514b
Autor:
Srilakshmi V. Patri, Srujan Marepally, Brijesh Lohchania, Venkatesh Ravula, Shireesha Manturthi, Venkanna Muripiti, Amarnath Velidandi
Publikováno v:
New Journal of Chemistry. 45:615-627
Cationic lipids have been effectively used as nonviral vectors for the delivery of polynucleic acids into the cytosol. In particular, lipids having hydroxy groups in the head group region facilitate the strong binding of polynucleic acids with the ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd78744e39177de05e525020401f1fbd
https://doi.org/10.1039/d0nj03717f
https://doi.org/10.1039/d0nj03717f
Autor:
G. V. P. Chandramouli, Srinivas Bandari, Amarnath Velidandi, Prasanna Bethanamudi, Kanakaraju Sankari
Publikováno v:
E-Journal of Chemistry, Vol 9, Iss 4, Pp 1676-1682 (2012)
The alkylation of 5-cyano indazoles 2 in the presence of readily available imidizolium salts (ionic liquids) (Bmim)BF4as phase transfer catalyst were performed to afford the regio isomersN1-andN2-(substituted alkyl)-5-cyano indazoles. TheN1-alkylated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c879da13ab0706ca7b5c08465af912a
https://doi.org/10.1155/2012/165784
https://doi.org/10.1155/2012/165784