The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole


Autoria(s): Pla Queral, Daniel; Mills, Keith; Joule, John A.; Albericio Palomera, Fernando; Álvarez Domingo, Mercedes
Contribuinte(s)

Universitat de Barcelona

Resumo

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

Identificador

http://hdl.handle.net/2445/62365

Idioma(s)

eng

Publicador

Michigan Publishing

Direitos

cc-by-nc (c) Pla Queral, Daniel et al., 2009

info:eu-repo/semantics/openAccess

<a href="http://creativecommons.org/licenses/by-nc/3.0/es">http://creativecommons.org/licenses/by-nc/3.0/es</a>

Palavras-Chave #Síntesi orgànica #Medicaments antineoplàstics #Compostos de nitrogen #Aziridines #Àcids nucleics #Organic synthesis #Antineoplastic agents #Nitrogen compounds #Aziridines #Nucleic acids
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion