A study of Heck cyclization reactions to form phenanthridine ring systems


Autoria(s): Donaldson, L.R.; Haigh, David; Hulme, A.N.
Data(s)

05/05/2008

Resumo

A survey of conditions for the palladium catalyzed intramol. Heck cyclization of protected amines has shown that the Herrmann-Beller palladacycle can be exploited under 'cationic' conditions to provide a robust and rapid route (

Identificador

http://pure.qub.ac.uk/portal/en/publications/a-study-of-heck-cyclization-reactions-to-form-phenanthridine-ring-systems(86c7f589-c975-4522-b45c-ebc5939547ff).html

http://dx.doi.org/10.1016/j.tet.2008.02.044

http://www.scopus.com/inward/record.url?scp=41549166001&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Donaldson , L R , Haigh , D & Hulme , A N 2008 , ' A study of Heck cyclization reactions to form phenanthridine ring systems ' Tetrahedron , vol 64 , no. 19 , pp. 4468-4477 . DOI: 10.1016/j.tet.2008.02.044

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1300/1303 #Biochemistry #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry #/dk/atira/pure/subjectarea/asjc/3000/3002 #Drug Discovery
Tipo

article