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- 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
- 210. The alkaloids of Mitragyne speciosa. Part I. Mitragynine. H. Raymond Ing, Clifford G. Raison
, J. Chem. Soc.
, 1939
, 986
- Total syntheses of mitragynine, paynantheine and speciogynine via an enantioselective thiourea-catalysed Pictet–Spengler reaction. Isabel P. Kerschgens, Elise Claveau, Martin J. Wanner, Steen Ingemann, Jan H. van Maarseveen, Henk Hiemstra
, Chem. Commun.
, 2012
, 48
, 12243
- An overview of recent developments in the analytical detection of new psychoactive substances (NPSs). Jamie P. Smith, Oliver B. Sutcliffe, Craig E. Banks
, Analyst
, 2015
, 140
, 4932
- 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
- Synthesis of indole derivatives as prevalent moieties present in selected alkaloids. Majid M. Heravi, Zahra Amiri, Kosar Kafshdarzadeh, Vahideh Zadsirjan
, RSC Adv.
, 2021
, 11
, 33540
- 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
- Enantioselective total syntheses of (−)-mitragynine, (−)-quinine and (+)-quinidine enabled by Ir-catalysed asymmetric hydrogenation of all-carbon tetrasubstituted cycloalkenes. Kai Zhang, Peng Cui, Miao Miao, Meiqi Zeng, Xu Wang, Minjie Zhang, Qifeng Chen, Hao Song, Bowen Ke, Yong Qin
, Org. Chem. Front.
, 2024
, 11
, 1456
- The cellular toxicology of mitragynine, the dominant alkaloid of the narcotic-like herb, Mitragyna speciosa Korth. Nor Aini Saidin, Elaine Holmes, Hiromitsu Takayama, Nigel J. Gooderham
, Toxicol. Res.
, 2015
, 4
, 1173
- Biosynthesis and synthetic biology of psychoactive natural products. Cooper S. Jamieson, Joshua Misa, Yi Tang, John M. Billingsley
, Chem. Soc. Rev.
, 2021
, 50
, 6950