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Please login to access the full content or check if you have access via31.15.4.1.3.2 Method 2: Synthesis from Dialkoxy(diaryl)sulfuranes
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Fernández, I.; Khiar, N., Science of Synthesis, (2007) 31, 1024.
Reactions between reactive sulfuranes and secondary alkylamines give azasulfonium salts. For example, the diphenylated sulfurane 68 [R1 = C(CF3)2Ph] combines with diisopropylamine to afford the corresponding (diisopropylamino)(diphenyl)sulfonium salt 69 [R1 = C(CF3)2Ph; R2 = iPr] (Scheme 42).[56]
Meeeee 88 (Meeeeeeeeeee)(eeeeeeee)eeeeeeeee Meeeeeeee eeee Meeeeeee(eeeeeeee)eeeeeeeeee[88]
Meeeeeeeeeee Meeeeeeee
(Meeeeeeeeeeeeeee)(eeeeeeee)eeeeeeeee 8,8,8,8,8,8-Meeeeeeeee-8-eeeeeeeeeeee-8-eeeee [88, M8 = M(MM8)8Me, M8 = eMe]; Meeeeee Meeeeeeee:[88]
Mee eeeeeeeee 88 [M8 = M(MM8)8Me; 8.88 e, 8.88 eeee] eee eeeeeee eeee eMe8MM (8 eM) eee ee eee eeeeee eeeeee e eee eee. Mee eeeeeee eee eeeeeee eeeeeeeee eee eeee eeeeee eeeee eee eeeeeee eeeee eeeeeee eeeeeeee ee eeeee e eeeeeeeeeee eeee. Meee eee eeeeeeeee eee eeeeeeeeeeeeee (MM8Me8/Me8M); eeeee: 8.88 e (88%); ee 888–888°M.
References
| [56] | Meeee, M. M.; Meeeee, M. M., M. Me. Meee. Mee., (8888) 88, 888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 88-8, 888.
- 8.Meeeee-Meee, (8888) M 88-8, 888.
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