
Tetrahedron p. 3005 - 3007 (1981)
Update date:2022-08-29
Topics:
Ashcroft, William R.
Martinez, Silvio J.
Joule, John, A.
Evidence bearing on the relative stabilities of 3- and 2-pyrrolines is reviewed.It is shown that 1-(indol-3-ylethyl)-3-pyrroline is only partially transformed into its enamine isomer by prolonged base treatment and it is concluded that within a 5-membered ring the allylamine is more stable than enamine.
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