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oai:docta.ucm.es:20.500.14352/1333712026-02-27T00:47:18Zcom_20.500.14352_14col_20.500.14352_15

Stereochemical issues related to the synthesis and reactivity of pyrazino[20 ,10 -5,1]pyrrolo[2,3-b]indole-1,4-diones Caballero, Esmeralda Avendaño López, María Carmen Menéndez, J. Carlos 547 Química orgánica (Farmacia) 2306 Química Orgánica The cyclization of all four diastereoisomers of cyclo-(Trp-Ala) to the corresponding 3,5a,6,10b,11,11ahexahydro-2H-pyrazino[20 ,10 -5,1]pyrrolo[2,3-b]indoles is studied from the stereochemical point of view. Epimerization of the tryptophan stereocenter during the cyclization and during acylation reactions of the N-2 atom of the tetracyclic derivatives is discussed. CICYT Depto. de Química Orgánica Fac. de Farmacia TRUE pub 2026-02-26T13:20:24Z 2026-02-26T13:20:24Z 1998 journal article VoR https://hdl.handle.net/20.500.14352/133371 XXXX-XXXX 10.1016/S0957-4166(98)00068-8 eng SAF-94-0517 SAF-97-0143 Caballero E, Avendaño C, Menéndez JC. Stereochemical issues related to the synthesis and reactivity of pyrazino[2′,1′-5,1]pyrrolo[2,3-b]indole-1,4-diones. Tetrahedron: Asymmetry. marzo de 1998;9(6):967-81. doi:10.1016/S0957-4166(98)00068-8 restricted access application/pdf Pergamon