Tetrahedron Letters p. 8687 - 8690 (1996)
Update date:2022-08-02
Topics:
Mastalerz, Harold
Doyle, Terrence W.
Kadow, John F.
Vyas, Dolatrai M.
An enediyne analog (2, R=H) that is a hybrid of the core structures of esperamicin and dynemicin was prepared. The key step in its synthesis was a Reissert-type reaction that involved intramolecular addition of the anion of a Z-1,3-diyn-2-ene to an N-acyl
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Doi:10.1021/ja01007a040
(1968)Doi:10.1039/CC9960002775
(1996)Doi:10.1021/je60037a051
(1968)Doi:10.1021/ja01047a020
(1969)Doi:10.1139/v96-219
(1996)Doi:10.1016/S0022-328X(96)06401-7
(1996)
