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- A novel method for source-specific hemoglobin adducts of nitro-polycyclic aromatic hydrocarbons. Kylie Wheelock, Junfeng (Jim) Zhang, Rob McConnell, Deliang Tang, Heather E. Volk, Ya Wang, Julie B. Herbstman, Shuang Wang, David H. Phillips, David Camann, Jicheng Gong, Frederica Perera
, Environ. Sci.: Processes Impacts
, 2018
, 20
, 780
- Dynamics and equilibrium for the formation of fluorescent Lewis acid–base exciplexes and triplexes between 9-aminophenanthrene and aliphatic amines. Frederick D. Lewis, Alvaro Ahrens, Todd L. Kurth
, Photochem. Photobiol. Sci.
, 2004
, 3
, 341
- Cp*Rh(iii)-catalyzed and solvent-controlled tunable [4 + 1]/[4 + 3] annulation for the divergent assembly of dihydrobenzo[cd]indoles and dihydronaphtho[1,8-bc]azepines. Zhuo-Zhuo Zhang, Ya Li, Bing-Feng Shi
, Org. Chem. Front.
, 2022
, 9
, 3262
- Carcinogenic nitrogen compounds. Part LXXV. Skraup reactions with some polycyclic amines, and two cases of anti-Marckwald orientation. N. P. Buu-Hoï, P. Jacquignon, D. C. Thang, T. Bartnik
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 263
- Carcinogenic nitrogen compounds. Part LVII. Hexacyclic acridines derived from phenanthrene and fluorene. D. C. Thang, Elizabeth K. Weisburger, Ph. Mabille, N. P. Buu-Hoï
, J. Chem. Soc. C
, 1967
, 665
- CLXXI.—The synthesis of complex acridines. Percy Corlett Austin
, J. Chem. Soc., Trans.
, 1908
, 93
, 1760
- The isolation-biological activities (2014–2022), bio, semi, total synthesis (1978–2022) and SAR studies of a potential naturally engineered scaffold aristolactam. Mallu Chenna Reddy, Ashutosh Dey, Masilamani Jeganmohan, Kishor Padala
, New J. Chem.
, 2023
, 47
, 16266
- CI.—Additive compounds of s-trinitrobenzene with amino-derivatives of complex aromatic hydrocarbons. Shunker Trimbak Cadre, John Joseph Sudborough
, J. Chem. Soc., Trans.
, 1916
, 109
, 1349
- Absorption and fluorescence spectral characteristics of aromatic amines in cetyltrimethylammonium bromide. Ranjit S. Sarpal, Sneh K. Dogra
, J. Chem. Soc., Faraday Trans.
, 1992
, 88
, 2725
- Monitoring intramolecular proton transfer with ion mobility-mass spectrometry and in-source ion activation. Younes Valadbeigi, Tim Causon
, Chem. Commun.
, 2023
, 59
, 1673