Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sreedhar Badvel"'
Autor:
Sreedhar, Badvel1, Reddy, Thummaluru Veera1, Raju, Chamarthi Naga2 rajuchamarthi10@gmail.com, Reddy, Gandi Vidya Sagar3
Publikováno v:
Organic Communications. Jul2016, Vol. 9 Issue 3, p54-64. 11p.
Autor:
Thaslim Basha Shaik, Raveendra Reddy Gopireddy, Sreedhar Badvel, Sudhamani Hasti, Veera Reddy Tummaluru, Naga Raju Chamarthi
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:749-753
A fast, efficient, and green synthesis of pyrimido[4,5-d]pyrimidine derivatives has been achieved via one-pot three-component reaction starting from 6-amino-N,N-dimethyluracil, phenylisothiocyanate or phenylisocyanate, and aromatic aldehydes in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2ac87bfe9370653a15b6eddf31080a0
https://doi.org/10.1007/s10593-015-1769-3
https://doi.org/10.1007/s10593-015-1769-3
Autor:
Sreedhar Badvel, Veera Reddy Tummaluru, Venugopal Reddy Katta, Vidya Sagar Reddy Gandi, Naga Raju Chamarthi, Padmavathi Venkatapuram
Publikováno v:
Organic Communications, Vol 8, Iss 2, Pp 43-51 (2015)
A series of new carboxamide derivatives of 3-(4-(5-(ethoxycarbonyl)-4-methylthiazol-2-yl)phenoxy)propionic acid were synthesized by Schotten-Baumann reaction. The newly synthesized compounds were characterized by IR, NMR and mass spectral analysis. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::24e75960a677562287e5aa07c1415277
Autor:
Sudhamani Hasti, Naga Raju Chamarthi, Raveendra Reddy Gopireddy, Thaslim Basha Shaik, Sreedhar Badvel, Veera Reddy Tummaluru
Publikováno v:
ChemInform. 47
A fast, efficient, and green synthesis of pyrimido[4,5-d]pyrimidine derivatives has been achieved via one-pot three-component reaction starting from 6-amino-N,N-dimethyluracil, phenylisothiocyanate or phenylisocyanate, and aromatic aldehydes in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd529603236f895f9b0095729cbbf3bf
https://doi.org/10.1002/chin.201614171
https://doi.org/10.1002/chin.201614171