Abstract
A straightforward synthesis of a structurally constrained C1-1′,2′,3′,4′-tetrahydro-1,1′- bisisoquinoline 1 is described. Resolution of this compound has been achieved successfully. The preparation of chiral N-alkyl, urea, and thiourea derivatives as potential new chiral ligands, based on the parent compound 1, is reported. Chiral compound 1 induced very good selectivity and yield in the addition of either Et2Zn (85% ee, 96% yield) or nitromethane (85% ee, 60% yield) to benzaldehyde.
Original language | English |
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Pages (from-to) | 4195-4205 |
Number of pages | 11 |
Journal | Tetrahedron |
Volume | 66 |
Issue number | 23 |
DOIs | |
Publication status | Published - Jun 5 2010 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Keywords
- Bischler-Napieralski reaction
- Bisisoquinolines
- C-C bond forming reactions
- Henry reaction