Reagent-Based DOS: Developing a Diastereoselective Methodology to Access Spirocyclic- and Fused Heterocyclic Ring Systems
- 7 August 2012
- journal article
- research article
- Published by Wiley in Chemistry – An Asian Journal
- Vol. 7 (10), 2351-2360
- https://doi.org/10.1002/asia.201200385
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Enantioselective synthesis of spirooxoindoles via chiral auxiliary (bicyclic lactam) controlled SNAr reactionsOrganic & Biomolecular Chemistry, 2010
- Diversity-oriented synthesis as a tool for the discovery of novel biologically active small moleculesNature Communications, 2010
- Stereochemical and Skeletal Diversity Arising from Amino Propargylic AlcoholsOrganic Letters, 2010
- Reagent based DOS: A “Click, Click, Cyclize” strategy to probe chemical spaceOrganic & Biomolecular Chemistry, 2010
- Asymmetric Cooperative Catalysis of Strong Brønsted Acid–Promoted Reactions Using Chiral UreasScience, 2010
- Aziridines as intermediates in diversity-oriented syntheses of alkaloidsTetrahedron Letters, 2009
- Multi-catalysis cascade reactions based on the methoxycarbonylketene platform: diversity-oriented synthesis of functionalized non-symmetrical malonates for agrochemicals and pharmaceuticalsOrganic & Biomolecular Chemistry, 2009
- Synthesis of Natural‐Product‐Like Molecules with Over Eighty Distinct ScaffoldsAngewandte Chemie-International Edition, 2008
- A ‘Rule of Three’ for fragment-based lead discovery?Drug Discovery Today, 2003
- 2-Carboxytetrahydroquinolines. Conformational and stereochemical requirements for antagonism of the glycine site on the N-methyl-D-aspartate (NMDA) receptorJournal of Medicinal Chemistry, 1992