You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via29.3.4.2.2 Method 2: Formation of α-Alkoxy Nitrogen Compounds
Please login to access the full content or check if you have access via
Benneche, T., Science of Synthesis, (2007) 29, 181.
Alkylation of 10H-quindoline (283) with iodomethyl methyl ether gives the 5-alkylated derivative 284 (Scheme 129);[327] no double alkylation occurs. Alkylation of quindoline under basic conditions gives the 10-alkylated isomer; quindoline cannot be alkylated under these conditions by bromomethyl methyl ether.[327]
Meeeee 888 Meeeeeeeee ee 88M-Meeeeeeeee[888]
Meeeeeeeeee Meeeeeeee
8-(Meeeeeeeeeeee)-88M-eeeeeeeeeeee Meeeee (888):[888]
M eeeeeee ee 88M-eeeeeeeeee (888, 8.888 e, 8.88 eeee) eee MMMM (8.88 eM) ee eeeeeee (88 eM) (MMMMMMM: eeeeeeeeee) eee eeeeeee ee ee eee 8 e eeeeee eeeee eeee e eeeeee eeeeeeeeeee eeeeee. Mee eeeeeee eee eeeeeeee eeeeeeee ee eeeeeeeeeeeeee (8–88% MeMM/MM8Me8 eeeeeeee); eeeee: 88%.
References
[327] | Mee, M.; Meeeeeeeeee, M. M., M. Meeeeeeeee. Meee., (8888) 88, 8888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 88e8, 888.