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(–)-Sparteine-mediated stereoselective directed ortho metalation of ferrocene diamides.
- Source :
-
Canadian Journal of Chemistry . Feb2006, Vol. 84 Issue 2, p356-369. 14p. 4 Diagrams, 6 Charts. - Publication Year :
- 2006
-
Abstract
- The utility of (–)-sparteine-mediated directed ortho metalation (DoM) has been investigated in stereoselective preparation of planar chiral ferrocenes derived from 1,1′-N,N,N′,N′-tetraisopropylferrocenedicarboxamide (5). In the synthesis of C2-symmetric analogs of 5, the protocol (base, solvent, and two-step DoM) was found to be crucial for obtaining high enantio- and diastereo-selectivities of the products. A variety of highly enantioenriched mono and doubly functionalized derivatives of 5 have been synthesized. The synthetic applications of these compounds as chiral ligands in asymmetric alkylation of aldehydes and asymmetric palladium-catalyzed allylic substitutions have been demonstrated. [ABSTRACT FROM AUTHOR]
- Subjects :
- *ORGANOMETALLIC chemistry
*SPARTEINE
*FERROCENE
*ALKYLATION
*ALDEHYDES
Subjects
Details
- Language :
- English
- ISSN :
- 00084042
- Volume :
- 84
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Canadian Journal of Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 20790393
- Full Text :
- https://doi.org/10.1139/V06-008