A Ring Rearrangement Approach to the Synthesis of Benzo[b]quinolizine and Benzoindolizine Architectures


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

01/06/2009

Resumo

An efficient ring rearrangement metathesis (RRM) approach to the synthesis of benzo[b]quinolizine and benzoindolizine systems from N-propargyl-phenanthridine derivatives is reported. A Hovel use of flash vacuum pyrolysis (FVP) for the Boc-deprotection of acid-sensitive substrates is also disclosed.

Identificador

http://pure.qub.ac.uk/portal/en/publications/a-ring-rearrangement-approach-to-the-synthesis-of-benzobquinolizine-and-benzoindolizine-architectures(3f0902e4-8478-4a2f-bf92-d9c776bb5026).html

http://dx.doi.org/10.1055/s-0029-1217338

http://www.scopus.com/inward/record.url?scp=67649406114&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Donaldson , L R , Haigh , D & Hulme , A N 2009 , ' A Ring Rearrangement Approach to the Synthesis of Benzo[b]quinolizine and Benzoindolizine Architectures ' Synlett , vol - , no. 10 , pp. 1587-1590 . DOI: 10.1055/s-0029-1217338

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry
Tipo

article