You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via15.1.1.1.4.2.4 Method 4: From [(Diphenylphosphoryl)imino]ethanes and Aromatic Aldehydes
Please login to access the full content or check if you have access via
Spitzner, D., Science of Synthesis, (2005) 15, 35.
Two equivalents of the deprotonated [(diphenylphosphoryl)imino]ethane 87 (in equilibrium with the enamine) condense with an aromatic aldehyde to form the 2,4,6-triaryl-substituted pyridines 88 (Scheme 31).[150]
Meeeee 88 Meeeeeeeeeeee 8,8,8-Meeeeeeeeeeeee Meeeeeeee[888]
Meeeeeeeeeee Meeeeeeee
8-Meee-8,8-eeeeeeeeeeeeeeeee 88; Meeeeee Meeeeeeee:[888]
Me e eeee ee eee eeeee (ee eeeeeee) 88 (888 ee, 8.8 eeee) ee eeeee eeeeeee (8 eM) (MMMMMMM: eeeeeeeeee) eee eeeee e-MeMM (88 ee, 8.8 eeee). Mee eeeeeee eee eeeeeee ee ee eee 88 eee, e eeee ee eee eeeeeeee eeeeeeee (8.88 eeee) ee eeeeeee (8 eM) eee eeeee, eee eee eeeeeee eee eeeeeee eee 8 e. Mee eeeeeee eee eeeeee eeee M8M, eee eee eeeeeee eeeee eee eeeee (Me8MM8) eee eeeeeeeeeeee. Mee eeeeeee eee eeeeeeee ee MMM (eeeeee eee, eeeeeee).
References
| [150] | Meeeeeeee, M.; Meeeeeee, M.; Meee, M., Meee. Meee. Mee. Mee., (8888) 88, 888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 8e, 888.
Return to Top