Scalable synthesis of enantiomerically pure bicyclo[2.2.2]octadiene ligands. | J Org Chem;77(10): 4765-73, 2012 May 18. | MEDLINE

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Scalable synthesis of enantiomerically pure bicyclo[2.2.2]octadiene ligands.

Abele, Stefan; Inauen, Roman; Spielvogel, Dirk; Moessner, Christian.

Affiliation

Abele S; Process Research Chemistry, Actelion Pharmaceuticals Ltd., Gewerbestrasse 16, CH-4123 Allschwil, Switzerland. stefan.abele@actelion.com

J Org Chem ; 77(10): 4765-73, 2012 May 18.

Article in En | MEDLINE | ID: mdl-22551166

Subject(s)

Acetaldehyde/analogs & derivatives; Bridged Bicyclo Compounds/chemistry; Bridged Bicyclo Compounds/chemical synthesis; Cyclohexanones/chemistry; Acetaldehyde/chemistry; Catalysis; Ligands; Molecular Structure; Stereoisomerism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bridged Bicyclo Compounds / Cyclohexanones / Acetaldehyde Language: En Journal: J Org Chem Year: 2012 Type: Article Affiliation country: Switzerland

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bridged Bicyclo Compounds / Cyclohexanones / Acetaldehyde Language: En Journal: J Org Chem Year: 2012 Type: Article Affiliation country: Switzerland