Cycloalkenyl Halide Substitution Reactions of Enantiopure Arene cis-Tetrahydrodiols with Boron, Nitrogen and Phosphorus Nucleophiles


Autoria(s): Boyd, D. R.; Sharma, N. D.; Kaik, M.; Bell, M.; Berberian, M. V.; McIntyre, P.B.A.; Kelly, B.; Hardacre, C.; Stevenson, P. J.; Allen, C. C. R.
Data(s)

01/09/2011

Resumo

Enantiopure arene cis-tetrahydrodiols of bromobenzene and iodobenzene have been obtained in good yields, from chemoselective hydrogenation (rhodium-graphite) of the corresponding cis-dihydrodiol metabolites. Palladium-catalysed substitution of the halogen, by hydrogen, boron, nitrogen and phosphorus nucleophiles, in the acetonide derivatives, has yielded highly functionalised products for application in synthesis with potential as scaffolds for chiral ligands.

Identificador

http://pure.qub.ac.uk/portal/en/publications/cycloalkenyl-halide-substitution-reactions-of-enantiopure-arene-cistetrahydrodiols-with-boron-nitrogen-and-phosphorus-nucleophiles(7521951e-7625-453e-9809-d14f0b31095d).html

http://dx.doi.org/10.1002/adsc.201100273

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Boyd , D R , Sharma , N D , Kaik , M , Bell , M , Berberian , M V , McIntyre , P B A , Kelly , B , Hardacre , C , Stevenson , P J & Allen , C C R 2011 , ' Cycloalkenyl Halide Substitution Reactions of Enantiopure Arene cis-Tetrahydrodiols with Boron, Nitrogen and Phosphorus Nucleophiles ' Advanced Synthesis & Catalysis , vol 353 , no. 13 , pp. 2455-2465 . DOI: 10.1002/adsc.201100273

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

article