Efficient access to enantiomerically pure rigid diamines
| Autor: | Loic Planas, Joelle Perard‐Viret, Jacques Royer |
|---|---|
| Přispěvatelé: | Chimie Organique, Médicinale et Extractive et Toxicologie Expérimentale (COMETE - UMR 8638), Université Paris Descartes - Paris 5 (UPD5)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Cibles Thérapeutiques et conception de médicaments (CiTCoM - UMR 8038), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP) |
| Rok vydání: | 2004 |
| Předmět: |
Addition reaction
[CHIM.ORGA]Chemical Sciences/Organic chemistry 010405 organic chemistry Organic Chemistry General Medicine 010402 general chemistry Combinatorial chemistry 01 natural sciences Catalysis Pyrrolidine 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound chemistry Michael reaction Organic chemistry Physical and Theoretical Chemistry Derivative (chemistry) |
| Zdroj: | Tetrahedron: Asymmetry Tetrahedron: Asymmetry, Elsevier, 2004, 15 (15), pp.2399-2403. ⟨10.1016/j.tetasy.2004.06.011⟩ |
| ISSN: | 0957-4166 |
| DOI: | 10.1016/j.tetasy.2004.06.011 |
| Popis: | International audience; Asymmetric spiro cyclization of a pyrrolidine derivative was used as a key step for constructing novel rigid diamines. Aselected example has proved its utility as a chiral nonmetallic catalyst in a Michael reaction. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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