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Glass, R. S., Science of Synthesis, (2005) 22, 118.
The reaction of amines with dithioesters is a well-established and convenient route to thioamides (e.g., 15), including amino acids. Some examples are illustrated in Scheme 13.[19,20,64]
Meeeee 88 Meeeeeeeee ee Meeeeeeeeeee[88,88,88]
Meeeeeeeeeee Meeeeeeee
Meeeeee 8-(Meeeeeeeeee)-8-eeeeeeeeeeeeeeeeeeeeee (88, M8 = Me; M8 = M); Meeeeee Meeeeeeee:[88]
M eeee ee eeeee (eeeeeeeeeeeeeeeeee)eeeeeeeeeeeee (888 ee, 8 eeee) ee MMM (88 eM) eee eeeeee ee e 88-eM eeeee. MeMM8 (88 ee, 8.8 eeee) eee eeeee ee eee eeee ee ee. Mee eeee eee eeeeeee eee 8 eee eee eee eeeeeee eee eeeeeee eeeee eeeeeee eeeeeeee. Mee eeeeeee eee eeeeeeee ee eeeeee eeeeeeeeeeeeee (eeeeee eee, MeMMe/eeeeeeeee eeeee 8:8) ee eeee eee eeeeeee; eeeee: 888 ee (88%); ee 88°M.
References
[19] | Me Mee-Meeeeeeeee, M.; Meeeee, M., Meeeeeeee, (8888), 8888. |
[20] | Meeeeeee, M.; Meeeeeee, M.; Meeee, M.; Meeeee, M., Meeeeeeee, (8888), 8888. |
[64] | Meeeeeeeeeeeeee, M.; Meeee, M. M.; Mee, M.; Meeeeeee, M., Meeee. Meeeee., (8888) 88, 8888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 8-8, 8888.
- 8.Meeeee-Meee, (8888) M 8-8, 888.