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- Highly conjugated architectures and labile reaction intermediates from coupling between 10π electron-deficient heteroaromatics and sym-trihydroxy- or triamino-benzene derivatives. Gabriele Micheletti, Carla Boga, Silvia Cino, Silvia Bordoni, Elena Chugunova
, RSC Adv.
, 2018
, 8
, 41663
- Energetic salts prepared from phenolate derivatives. Dharavath Srinivas, Vikas D. Ghule, Krishnamurthi Muralidharan
, New J. Chem.
, 2014
, 38
, 3699
- Photo-responsive molecularly imprinted hydrogels for the detection of melamine in aqueous media. Qian Tang, Ying-Tian Nie, Cheng-Bin Gong, Cheuk-Fai Chow, Jing-Dong Peng, Michael Hon-Wah Lam
, J. Mater. Chem.
, 2012
, 22
, 19812
- Conductive two-dimensional M3(C6S3O3)2 monolayers as effective electrocatalysts for the oxygen reduction reaction. Tianchun Li, Manman Li, Xinyue Zhu, Juan Zhang, Yu Jing
, J. Mater. Chem. A
, 2021
, 9
, 24887
- Effects of colonic fermentation on the stability of fresh and black onion bioactives. Alicia Moreno-Ortega, Giuseppe Di Pede, Pedro Mena, Luca Calani, Daniele Del Rio, José Manuel Moreno-Rojas, Gema Pereira-Caro
, Food Funct.
, 2022
, 13
, 4432
- Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light. Ignacio D. Lemir, Willber D. Castro-Godoy, Adrián A. Heredia, Luciana C. Schmidt, Juan E. Argüello
, RSC Adv.
, 2019
, 9
, 22685
- Phloroglucinol compounds of natural origin: Synthetic aspects. Inder Pal Singh, Jasmeen Sidana, Sandip B. Bharate, William J. Foley
, Nat. Prod. Rep.
, 2010
, 27
, 393
- Co-crystallization of oxadiazole-bridged pyridyl-N-oxide building modules with R-aromatics (R = –OH, –NH2 and –COOH). Gui-Ge Hou, Jian-Ping Ma, Le Wang, Ping Wang, Yu-Bin Dong, Ru-Qi Huang
, CrystEngComm
, 2010
, 12
, 4287
- Characterization of LiNi0.5Mn1.5O4 spinel electrode in the presence of 1,3,5-trihydroxybenzene as additive. Alexis Perea, Karim Zaghib, Daniel Bélanger
, J. Mater. Chem. A
, 2015
, 3
, 2776
- Phloroglucinol-encapsulated starch biopolymer: preparation, antioxidant and cytotoxic effects on HepG2 liver cancer cell lines. Ponnuchamy Kumar, Singaravelu Senthamilselvi, Munisamy Govindaraju
, RSC Adv.
, 2014
, 4
, 26787