A Facile Route of Synthesis for Making Flibanserin
- 12 August 2016
- journal article
- Published by American Chemical Society (ACS) in Organic Process Research & Development
- Vol. 20 (9), 1576-1580
- https://doi.org/10.1021/acs.oprd.6b00108
Abstract
No abstract availableFunding Information
- Ministry of Science and Technology of the People's Republic of China (2013ZX09507001)
This publication has 9 references indexed in Scilit:
- Flibanserin: First Global ApprovalDrugs, 2015
- Flibanserin for the treatment of hypoactive sexual desire disorder in premenopausal womenExpert Opinion on Pharmacotherapy, 2015
- Discovery and Optimization of Small-Molecule Ligands for the CBP/p300 BromodomainsJournal of the American Chemical Society, 2014
- A Practical and Convenient Method for the Synthesis of Some BenzimidazolesOrganic Preparations and Procedures International, 2013
- Functional Dihydro-1H-Imidazole Derivatives for MALDI Signal Enhancement of a Lysine-Specific Chemical ModificationJournal of the Chinese Chemical Society, 2009
- Benzimidazole-substituted (3-phenoxypropyl)amines as histamine H3 receptor ligandsBioorganic & Medicinal Chemistry Letters, 2008
- Design, synthesis, and cytotoxicity of 4-sulfonamide substituted benzamidobenzimidazolones and an acyl benzimidazoloneJournal of the Iranian Chemical Society, 2005
- Nouvelle synthese des benzodiazepines-1,5 a partir de la γ-pyroneTetrahedron Letters, 1987
- Synthesis of 1‐alkyl and 1,3‐dialkyl‐2‐benzimidazolones from 1‐alkenyl‐2‐benzimidazolones using phase‐transfer catalysis techniqueJournal of Heterocyclic Chemistry, 1981