Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Chandrasekar Balachandran"'
Autor:
Chennakesava Rao Kella, Chandrasekar Balachandran, Yuvaraj Arun, Easwaramoorthi Kaliyappan, Sakkarapalayam M. Mahalingam, Savarimuthu Ignacimuthu, Natarajan Arumugam, Abdulrahman I. Almansour, Raju Suresh Kumar, Paramasivan T. Perumal
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 12, Pp 9047-9057 (2020)
A Novel class of 1,4-disubstituted 1,2,3-triazoles have been synthesized in good to excellent yields via Cu(I) accelerated azide-alkyne click chemistry reaction strategy. The newly synthesized compounds were assessed for their in vitro antimicrobial
Externí odkaz:
https://doaj.org/article/445115270305406a82ff724b210f4bab
Autor:
Govindhan Muniyappan, Subramanian Kathavarayan, Chandrasekar Balachandran, Easwaramoorthi Kalliyappan, Sakkarapalayam M. Mahalingam, Abdul Ajees Abdul Salam, Shin Aoki, Natarajan Arumugam, Abdulrahman I. Almansour, Raju Suresh Kumar
Publikováno v:
Journal of King Saud University: Science, Vol 32, Iss 8, Pp 3286-3292 (2020)
A small library of hitherto unexplored novel 5-fluorobenzoisoxazolyl-piperidinyl-1, 2, 3-triazole derivatives has been synthesized from 2-azido-fluorobenzoisoxazolyl piperidinyl ethanone and various alkynes in good to excellent yields through a click
Externí odkaz:
https://doaj.org/article/ae65e9ab47524d0fb61e15feef2fe346
Autor:
Kenta Yokoi, Chandrasekar Balachandran, Masakazu Umezawa, Koji Tsuchiya, Aleksandra Mitrić, Shin Aoki
Publikováno v:
ACS Omega, Vol 5, Iss 12, Pp 6983-7001 (2020)
Externí odkaz:
https://doaj.org/article/22a74c9d37cb4574a76d30f29703bf1e
Autor:
Mathiyan Muralisankar, Ramachandran Dheepika, Jebiti Haribabu, Chandrasekar Balachandran, Shin Aoki, Nattamai S. P. Bhuvanesh, Samuthira Nagarajan
Publikováno v:
ACS Omega, Vol 4, Iss 7, Pp 11712-11723 (2019)
Externí odkaz:
https://doaj.org/article/bc6bb20c6cd642cbb5530787542d551d
Autor:
Chandrasekar Balachandran, Kenta Yokoi, Kana Naito, Jebiti Haribabu, Yuichi Tamura, Masakazu Umezawa, Koji Tsuchiya, Toshitada Yoshihara, Seiji Tobita, Shin Aoki
Publikováno v:
Molecules, Vol 26, Iss 22, p 7028 (2021)
In our previous paper, we reported that amphiphilic Ir complex–peptide hybrids (IPHs) containing basic peptides such as KK(K)GG (K: lysine, G: glycine) (e.g., ASb-2) exhibited potent anticancer activity against Jurkat cells, with the dead cells sho
Externí odkaz:
https://doaj.org/article/e56603c0095a4cdfba9e31644617f6d3
Autor:
Sivakalai Mayakrishnan, Yuvaraj Arun, Chandrasekar Balachandran, Suresh Awale, Narayanan Uma Maheswari, Paramasivan Thirumalai Perumal
Publikováno v:
ACS Omega, Vol 2, Iss 6, Pp 2694-2705 (2017)
Externí odkaz:
https://doaj.org/article/8886a948efff46a4ba9ef61b8a81b0b4
Autor:
Kaliyappan Easwaramoorthi, Jeya A. Rajendran, Kella Chennakesava Rao, Chandrasekar Balachandran, Yuvaraj Arun, Sakkarapalayam M. Mahalingam, Natarajan Arumugam, Abdulrahman I. Almansour, Raju Suresh Kumar, Dhaifallah M. Al-thamili, Shin Aoki
Publikováno v:
Molecules, Vol 24, Iss 19, p 3501 (2019)
New 1,4-disubstituted β-pyrrolidino-1,2,3-triazoles were synthesized using a reusable copper-iodide-doped neutral alumina catalyst. Synthesis of diversely substituted triazoles and recyclability of CuI catalyst explains the broad scope of this proto
Externí odkaz:
https://doaj.org/article/037805d8f0d24e159b43073ef92409a3
Autor:
Paramasivan T. Perumal, Narayanan Uma Maheswari, Mahalingam Sivaraman, Sivakalai Mayakrishnan, Chandrasekar Balachandran, Shin Aoki
Publikováno v:
Synlett. 33:785-790
Privileged indole-fused phenanthridinones were synthesized by an inexpensive potassium tert-butoxide-promoted intramolecular Mizoroki–Heck-type radical cyclization. This method offers high atom- and step-economic C–C bond formation. An array of t
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 79:1113-1124
Autor:
Shin Aoki, Kenta Yokoi, Yosuke Hisamatsu, Chandrasekar Balachandran, Yuichi Tamura, Tomohiro Tanaka
Publikováno v:
Metal Ligand Chromophores for Bioassays ISBN: 9783031198625
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc6cf4d9a370a23f4e6d40722a40dad0
https://doi.org/10.1007/978-3-031-19863-2_5
https://doi.org/10.1007/978-3-031-19863-2_5