Results
1 -
10 of
513
(Click
here to explore results)
- Syntheses of the plant auxin conjugate 2-O-(indole-3-acetyl)-myo-inositol IAInos. Saúl Silva, Osvaldo S. Ascenso, Eva C. Lourenço, Margarida Archer, Christopher D. Maycock, M. Rita Ventura
, Org. Biomol. Chem.
, 2018
, 16
, 6860
- Effects of theabrownin on serum metabolites and gut microbiome in rats with a high-sugar diet. Suijuan Yue, Dan Zhao, Chunxiu Peng, Chao Tan, Qiuping Wang, Jiashun Gong
, Food Funct.
, 2019
, 10
, 7063
- Development of a continuous flow synthesis of FGIN-1-27 enabled by in-line 19F NMR analyses and optimization algorithms. N. Vasudevan, Ehu C. Aka, Elvina Barré, Eric Wimmer, Daniel Cortés-Borda, Patrick Giraudeau, Jonathan Farjon, Mireia Rodriguez-Zubiri, François-Xavier Felpin
, React. Chem. Eng.
, 2021
, 6
, 1983
- Naturally based ionic liquids with indole-3-acetate anions and cations derived from cinchona alkaloids. Tomasz Rzemieniecki, Tomasz Kleiber, Juliusz Pernak
, RSC Adv.
, 2021
, 11
, 27530
- Nonionic nontoxic antimicrobial polymers: indole-grafted poly(vinyl alcohol) with pendant alkyl or ether groups. Xiaoya Li, Sedef İlk, Yang Liu, Deepak Bushan Raina, Deniz Demircan, Baozhong Zhang
, Polym. Chem.
, 2022
, 13
, 2307
- N-Containing compounds of macromycetes. Meng-Yuan Jiang, Tao Feng, Ji-Kai Liu
, Nat. Prod. Rep.
, 2011
, 28
, 783
- A general strategy for the synthesis of indoloquinolizine alkaloids via a cyanide-catalyzed imino-Stetter reaction. Eunjoon Park, Cheol-Hong Cheon
, Org. Biomol. Chem.
, 2017
, 15
, 10265
- A cyanide-catalyzed imino-Stetter reaction enables the concise total syntheses of rucaparib. Jinjae Park, Cheol-Hong Cheon
, RSC Adv.
, 2022
, 12
, 21172
- 418. Synthesis of indoleacetic acids. Frederick E. King, Philibert L'Ecuyer
, J. Chem. Soc.
, 1934
, 1901
- Propionate as the preferred carbon source to produce 3-indoleacetic acid in B. subtilis: comparative flux analysis using five carbon sources. Freddy Castillo Alfonso, Gabriel Vigueras-Ramírez, Luis Manuel Rosales-Colunga, Alberto del Monte-Martínez, Roberto Olivares Hernández
, Mol. Omics
, 2021
, 17
, 554