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Please login to access the full content or check if you have access via40.1.4 Product Subclass 4: n-Nitrogen- or n-Phosphorus-Functionalized Alkylamines (n ≥2)
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DOI:
10.1055/sos-SD-040-00411
Roy, K.-M., Science of Synthesis, (2009) 40, 615.
General Introduction
1,n-Diamines (n ≥2) can be prepeared by various addition reactions across C—C and C—N bonds, including amination of dienes and alkenes, ring opening of aziridines and azetidines with amines or azides, and coupling reactions of nitrogen compounds such as imines and amines. These methods have been reviewed in Houben–Weyl, Vol. E 16d, pp 791, 808, 1127, 1169, and Vol. E 21d, pp 5325, 5361, 5372, 5693, as well as in other series and journals.[1,2] The formation of 1,3-diamines by catalytic reductive cleavage of cyclic hydrazines is discussed in Section 40.1.1.1.5.9[3]
References
| [1] | Meeeee, M. M.; Meee, M., Me Meeeeeeeeeeee Meeeeee Meeeeeeeee Meeee Meeeeeeeeeeeeee MM, Meeeeeeee, M. M.; Meeeee, M. M. M., Mee.; Meeeeeee: Meeeee, (8888); Mee. 8, e 888. |
| [2] | Meeee, M.; Me Meee, M.; Meeeeeeeee, M., Meeee. Meee., (8888) 888, 8888; Meeee. Meee. Mee. Me., (8888) 88, 8888. |
| [3] | Meeee, M.; Meeee, M.; Meeeee, M.; Meeeee, M., M. Mee. Meee., (8888) 88, 888. |
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- 8.Meeeee-Meee, (8888) M 88e, 8888.
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