Synthesis, enantiomer separation, and absolute configuration of 2,6-oxygenated 9-azabicyclo[3.3.1]nonanes. | J Org Chem;78(11): 5339-48, 2013 Jun 07. | MEDLINE

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Synthesis, enantiomer separation, and absolute configuration of 2,6-oxygenated 9-azabicyclo[3.3.1]nonanes.

Bieliunas, Vidmantas; Rackauskaite, Dovile; Orentas, Edvinas; Stoncius, Sigitas.

Affiliation

Bieliunas V; Department of Organic Chemistry, Vilnius University, Naugarduko 24, 03225 Vilnius, Lithuania.

J Org Chem ; 78(11): 5339-48, 2013 Jun 07.

Article in En | MEDLINE | ID: mdl-23635000

Subject(s)

Azabicyclo Compounds; Oxygen/chemistry; Azabicyclo Compounds/chemical synthesis; Azabicyclo Compounds/chemistry; Azabicyclo Compounds/isolation & purification; Molecular Structure; Quantum Theory; Stereoisomerism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Azabicyclo Compounds Language: En Journal: J Org Chem Year: 2013 Type: Article Affiliation country: Lithuania

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Azabicyclo Compounds Language: En Journal: J Org Chem Year: 2013 Type: Article Affiliation country: Lithuania