HAL Science
metadata only
Driving the Morita-Baylis-Hillman Reaction to a Multicomponent Organic Transformation
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
- Computational elucidation of chemical transformations in biochemically active molecules: from NMR chemical shifts to reaction pathways / Judit Katalin Szántó ; Betreuer: Christian Ochsenfeld#661769
- Skeletal Editing via Diastereoselective Ring Expansion Enables Enantioenriched Tetrasubstituted Δ 3 -Oxepenes#357549
- Conflict-Aware Harmonized Rotational Gradient for Multiscale Kinetic Regimes#138908
- Synthesis of 5,5-Disubstituted Butenolides Based on a Pd-Catalyzed γ-Arylation Strategy#367752
- Development of an Enantioselective Synthesis of (–)-Euonyminol and Studies Towards the Total Synthesis of (–)-Lomaiviticin A#673219
Record · ID 635091
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