Journal of Organic Chemistry p. 2229 - 2231 (1982)
Update date:2022-08-02
Topics: Nucleophilic substitution Novel Chemical Synthesis Heterocyclic Chemistry Spectroscopic Analysis Entry Indole alkaloids Alkaloid biosynthesis
Meyers, A. I.
Hellring, Stuart
By use of α-amino carbanions generated from β-carbolines and the succesful blocking of indole nitrogen, the elaboration of these systems to indole alkaloids is described.
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Doi:10.1016/S0040-4039(01)93030-8
(1981)Doi:10.1016/S0040-4039(00)86790-8
(1982)Doi:10.1021/ja00377a027
(1982)Doi:10.1016/S0040-4039(01)92481-5
(1981)Doi:10.1016/j.bmc.2014.04.003
(2014)Doi:10.1016/S0008-6215(00)88059-3
(1982)