Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-Dimethylglutaric Anhydride


Autoria(s): Cook, Matthew; Rovis, T.
Data(s)

16/01/2009

Resumo

A rhodium-catalyzed enantioselective cross-coupling of sp³ organozinc reagents and 3,5-dimethylglutaric anhydride has been developed to afford the corresponding products, syn-deoxypolypropionates, in excellent yields and enantioselectivities. This reaction has been developed so that both commercially available and in situ prepared organozinc reagents are competent coupling partners.

Identificador

http://pure.qub.ac.uk/portal/en/publications/enantioselective-rhodiumcatalyzed-alkylative-desymmetrization-of-35dimethylglutaric-anhydride(4a1bae7e-6aa7-4722-aec9-3b08647b3058).html

http://dx.doi.org/10.1055/s-0028-1083275

http://www.scopus.com/inward/record.url?scp=63849165802&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Cook , M & Rovis , T 2009 , ' Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-Dimethylglutaric Anhydride ' Synthesis , vol 2 , no. 2 , pp. 335-338 . DOI: 10.1055/s-0028-1083275

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1500/1503 #Catalysis #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry
Tipo

article