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- Total synthesis of the pseudoindoxyl class of natural products. Pawan S. Dhote, Pitambar Patel, Kumar Vanka, Chepuri V. Ramana
, Org. Biomol. Chem.
, 2021
, 19
, 7970
- A chemical synthesis of 11-methoxy mitragynine
pseudoindoxyl featuring the interrupted Ugi reaction. Jimin Kim, John S. Schneekloth, Erik J. Sorensen
, Chem. Sci.
, 2012
, 3
, 2849
- dppb and TfOH promoted cascade reaction of o-nitrophenylpropiolamides to access C2-spiro-pseudoindoxyls. Qiongwen Kang, Yan Wang, Zongkang Wang, Nana Fei, Peng He, Lingkai Kong, Yanzhong Li
, Org. Chem. Front.
, 2024
, 11
, 2075
- Biosynthesis and synthetic biology of psychoactive natural products. Cooper S. Jamieson, Joshua Misa, Yi Tang, John M. Billingsley
, Chem. Soc. Rev.
, 2021
, 50
, 6950
- Comprehensive overview of biased pharmacology at the opioid receptors: biased ligands and bias factors. Jolien De Neve, Thomas M. A. Barlow, Dirk Tourwé, Frédéric Bihel, Frédéric Simonin, Steven Ballet
, RSC Med. Chem.
, 2021
, 12
, 828
- Recent advances in the synthesis of C2-spiropseudoindoxyls. Yanling Ji, Xianghong He, Cheng Peng, Wei Huang
, Org. Biomol. Chem.
, 2019
, 17
, 2850
- Pd-Catalyzed cycloisomerization/nucleophilic addition/reduction: an efficient method for the synthesis of spiro-pseudoindoxyls containing N,N′-ketal. Lin-Wei Chen, Jia-Lin Xie, Hong-Jian Song, Yu-Xiu Liu, Yu-Cheng Gu, Qing-Min Wang
, Org. Chem. Front.
, 2017
, 4
, 1731
- Facile access to 2,2-disubstituted indolin-3-ones via a cascade Fischer indolization/Claisen rearrangement reaction. Zilei Xia, Jiadong Hu, Yu-Qi Gao, Qizheng Yao, Weiqing Xie
, Chem. Commun.
, 2017
, 53
, 7485
- An efficient method to access spiro pseudoindoxyl ketones: evaluation of indoxyl and their N-benzylated derivatives for inhibition of the activity of monoamine oxidases. Karuppaiah Perumal, Jiseong Lee, Sesuraj Babiola Annes, Subburethinam Ramesh, T. M. Rangarajan, Bijo Mathew, Hoon Kim
, RSC Adv.
, 2023
, 13
, 24925
- Natural product modulators of human sensations and mood: molecular mechanisms and therapeutic potential. Tomáš Pluskal, Jing-Ke Weng
, Chem. Soc. Rev.
, 2018
, 47
, 1592