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- Dioxygen reactivity of iron(ii)–gentisate/1,4-dihydroxy-2-naphthoate complexes of N4 ligands: oxidative coupling of 1,4-dihydroxy-2-naphthoate. Rubina Rahaman, Sandip Munshi, Sridhar Banerjee, Biswarup Chakraborty, Sarmistha Bhunia, Tapan Kanti Paine
, Dalton Trans.
, 2019
, 48
, 16993
- Fluorescence excitation and excited state intramolecular proton transfer of jet-cooled naphthol derivatives: Part 1. 1-hydroxy-2-naphthaldehyde. Annemarie McCarthy, Albert A. Ruth
, Phys. Chem. Chem. Phys.
, 2011
, 13
, 7485
- Prototropic forms of hydroxy derivatives of naphthoic acid within deep eutectic solvents. Vaishali Khokhar, Siddharth Pandey
, Phys. Chem. Chem. Phys.
, 2021
, 23
, 9096
- Utility of 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole for development of a highly sensitive stability indicating spectrofluorimetric method for determination of salmeterol xinafoate; application to human plasma. Mahmoud A. Omar, Mohamed A. Hammad, Mohamed Awad
, RSC Adv.
, 2017
, 7
, 44773
- Biocatalytic CO2 fixation initiates selective oxidative cracking of 1-naphthol under ambient conditions. Pengju Ren, Zijian Tan, Yingying Zhou, Hongzhi Tang, Ping Xu, Haifeng Liu, Leilei Zhu
, Green Chem.
, 2022
, 24
, 4766
- Effects of π-expansion, an additional hydroxyl group, and substitution on the excited state single and double proton transfer of 2-hydroxybenzaldehyde and its relative compounds: TD-DFT static and dynamic study. Chanatkran Prommin, Khanittha Kerdpol, Tinnakorn Saelee, Nawee Kungwan
, New J. Chem.
, 2019
, 43
, 19107
- CCCXXXIV.—Optical activity and the polarity of substituent groups. Part XII. The direct space effects of meta and ortho-para directive substituents. l-Menthyl esters of substituted naphthoic acids. H. Gordon Rule, John Spence, Egon Bretscher
, J. Chem. Soc.
, 1929
, 2516
- Advanced design and development of nanoparticle/microparticle dual-drug combination lactose carrier-free dry powder inhalation aerosols. Priya Muralidharan, Evan K. Mallory, Monica Malapit, Hanna Phan, Julie G. Ledford, Don Hayes, Heidi M. Mansour
, RSC Adv.
, 2020
, 10
, 41846
- The chemotherapy of tuberculosis. Part V. Some 5-amino-benzacridines and -dibenzacridines. J. Cymerman-Craig, J. W. Loder
, J. Chem. Soc.
, 1955
, 4309
- A highly efficient kinetic resolution of Morita–Baylis–Hillman adducts achieved by N–Ar axially chiral Pd-complexes catalyzed asymmetric allylation. Feijun Wang, Shengke Li, Mingliang Qu, Mei-Xin Zhao, Lian-Jun Liu, Min Shi
, Chem. Commun.
, 2011
, 47
, 12813