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- Pd(OAc)2-catalysed regioselective alkoxylation of aryl (β-carbolin-1-yl)methanones via β-carboline directed ortho-C(sp2)–H activation of an aryl ring. Shivalinga Kolle, Sanjay Batra
, Org. Biomol. Chem.
, 2015
, 13
, 10376
- TCCA-mediated oxidative rearrangement of tetrahydro-β-carbolines: facile access to spirooxindoles and the total synthesis of (±)-coerulescine and (±)-horsfiline. Manda Sathish, Akash P. Sakla, Fabiane M. Nachtigall, Leonardo S. Santos, Nagula Shankaraiah
, RSC Adv.
, 2021
, 11
, 16537
- Medium-sized and strained heterocycles from non-catalysed and gold-catalysed conversions of β-carbolines. Sandra Medina, Álvaro González-Gómez, Gema Domínguez, Javier Pérez-Castells
, Org. Biomol. Chem.
, 2012
, 10
, 7167
- Copper-catalyzed oxidative cleavage of Passerini and Ugi adducts in basic medium yielding α-ketoamides. Anirban Ghoshal, Mayur D. Ambule, Revoju Sravanthi, Mohit Taneja, Ajay Kumar Srivastava
, New J. Chem.
, 2019
, 43
, 14459
- Reusable, homogeneous water soluble photoredox catalyzed oxidative dehydrogenation of N-heterocycles in a biphasic system: application to the synthesis of biologically active natural products. S. Srinath, R. Abinaya, Arun Prasanth, M. Mariappan, R. Sridhar, B. Baskar
, Green Chem.
, 2020
, 22
, 2575
- Silylacetate-promoted addition reaction of isocyanides to nitrones: effective synthesis of C(1)-carboxamide derivatives. Takahiro Soeta, Siming Yao, Hirokazu Sugiyama, Yutaka Ukaji
, Org. Biomol. Chem.
, 2024
, 22
, 1619
- Condensation of anthranilic acids with pyridines to furnish pyridoquinazolones via pyridine dearomatization. Yajun Yang, Cuiju Zhu, Min Zhang, Shijun Huang, Jingjing Lin, Xiandao Pan, Weiping Su
, Chem. Commun.
, 2016
, 52
, 12869
- IBX-mediated oxidative addition of isocyanides to cyclic secondary amines: total syntheses of alangiobussine and alangiobussinine. Mayur D. Ambule, Shashank Tripathi, Anirban Ghoshal, Ajay K. Srivastava
, Chem. Commun.
, 2019
, 55
, 10872
- The rapid profiling and simultaneous determination of 12 major alkaloids in Nauclea officinalis by UPLC-Q-TOF-MS and HPLC-ESI-MS/MS. Guanghou Wang, Hongjin Wang, Huan Liu, Yue Wang, Ziwei Lin, Lixin Sun
, Anal. Methods
, 2021
, 13
, 5787