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- Suspect and non-target screening of ovarian follicular fluid and serum – identification of anthropogenic chemicals and investigation of their association to fertility. Ida Hallberg, Merle Plassmann, Matts Olovsson, Jan Holte, Pauliina Damdimopoulou, Ylva C. B. Sjunnesson, Jonathan P. Benskin, Sara Persson
, Environ. Sci.: Processes Impacts
, 2021
, 23
, 1578
- 324. The chemistry of bacteria. Part I. The synthesis of hydroxyindoles. R. J. S. Beer, Kenneth Clarke, H. G. Khorana, Alexander Robertson
, J. Chem. Soc.
, 1948
, 1605
- 6-Hydroxyindole-based borondipyrromethene: Synthesis and spectroscopic studies. Chunchang Zhao, Peng Feng, Jian Cao, Yulin Zhang, Xuzhe Wang, Yang Yang, Yanfen Zhang, Jinxin Zhang
, Org. Biomol. Chem.
, 2012
, 10
, 267
- Borondipyrromethene-derived Cu2+ sensing chemodosimeter for fast and selective detection. Chunchang Zhao, Peng Feng, Jian Cao, Xuzhe Wang, Yang Yang, Yulin Zhang, Jinxing Zhang, Yanfen Zhang
, Org. Biomol. Chem.
, 2012
, 10
, 3104
- A colorimetric and ratiometric NIR fluorescent turn-on fluoride chemodosimeter based on BODIPY derivatives: high selectivity via specific Si–O cleavage. Jian Cao, Chunchang Zhao, Peng Feng, Yulin Zhang, Weihong Zhu
, RSC Adv.
, 2012
, 2
, 418
- Target-triggered deprotonation of 6-hydroxyindole-based BODIPY: specially switch on NIR fluorescence upon selectively binding to Zn2+. Jian Cao, Chunchang Zhao, Xuzhe Wang, Yanfen Zhang, Weihong Zhu
, Chem. Commun.
, 2012
, 48
, 9897
- An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy. Bei Zhou, Zhi-Cheng Liu, Wen-Wen Qu, Rui Yang, Xin-Rong Lin, Sheng-Jiao Yan, Jun Lin
, Green Chem.
, 2014
, 16
, 4359
- 668. The structure and properties of certain polycyclic indolo- and quinolino-derivatives. Part IX. Derivatives of 1 : 3 : 4 : 5-tetrahydro-5-oxobenz[cd]indole. Frederick G. Mann, A. J. Tetlow
, J. Chem. Soc.
, 1957
, 3352
- Regioselective Claisen rearrangements in indoles. Christopher J. Moody
, J. Chem. Soc., Chem. Commun.
, 1983
, 1129
- Dynamics of electronically excited states in the eumelanin building block 5,6-dihydroxyindole. Stuart W. Crane, Omair Ghafur, Thomas Y. Cowie, Anita G. Lindsay, James O. F. Thompson, Jason B. Greenwood, Magnus W. P. Bebbington, Dave Townsend
, Phys. Chem. Chem. Phys.
, 2019
, 21
, 8152