Aziridines as intermediates in diversity-oriented syntheses of alkaloids
- 10 February 2009
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 50 (26), 3230-3233
- https://doi.org/10.1016/j.tetlet.2009.02.034
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Molecular diversity by designNature, 2009
- Towards the Optimal Screening Collection: A Synthesis StrategyAngewandte Chemie International Edition, 2007
- Drugs for bad bugs: confronting the challenges of antibacterial discoveryNature Reviews Drug Discovery, 2006
- Facile Regio- and Stereoselective Carbon−Carbon Coupling of Phenol Derivatives with Aryl AziridinesOrganic Letters, 2006
- Substituents Effect on Aziridine Chemistry: N-Inversion Energy, Reactivity and Regioselectivity of Nucleophilic Ring-openingBulletin of the Korean Chemical Society, 2005
- The Brønsted Acid-Catalyzed Direct Aza-Darzens Synthesis of N-Alkyl cis-AziridinesJournal of the American Chemical Society, 2004
- A Planning Strategy for Diversity‐Oriented SynthesisAngewandte Chemie International Edition, 2003
- Lewis acid promoted regio- and stereoselective hetero nucleophilic addition to a piperidinyl aziridine. Synthesis of trans 3-amino-4-substituted piperidinesTetrahedron Letters, 2002
- Target-Oriented and Diversity-Oriented Organic Synthesis in Drug DiscoveryScience, 2000
- Ab Initio Study of Aziridines and Diaziridines: Nitrogen Inversion, Ring Opening, and ThermochemistryThe Journal of Physical Chemistry A, 1998