HAL (France)
open access
Chiral phosphoric acid-catalyzed construction of azacyclic compounds
Chiral azaheterocycles are valuable unitswidely found in various natural products, and biologicallyactive substances. The cycloaddition is considered as oneof the most direct and efficient strategy for the preparationthem. Organocatalysis relying on Brønsted acid catalystssuch as BINOL-derived phosp
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Enantioselective synthesis of chiral azacyclohexenone precursors.#646212
- The structure of symmetric azoazoles according to ab initio computations#1166148
- Chiral (Stereoselective) Drugs, Asymmetric Synthesis, and Racemic Resolution Methods.#295134
- Access to Chiral Cyclic β‐Enaminones via Enantioselective Imine Condensation#454752
- The Quest for Secondary Pharmaceuticals: Drug Repurposing/Chiral-Switches Combination Strategy#270997
Record · ID 1203793
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive