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Volumn 46, Issue 3, 2005, Pages 509-512

Corrigendum to "Preparation of chiral 7,7′-disubstituted BINAPs for Rh-catalyzed 1,4-addition of arylboronic acids". [Tetrahedron Lett. 46 (2005) 509] (DOI:10.1016/j.tetlet.2004.11.096);Preparation of chiral 7,7′-disubstituted BINAPs for Rh-catalyzed 1,4-addition of arylboronic acids

Author keywords

1,4 Addition; 7,7 Disubstituted BINAP; Arylboronic acids; Asymmetric catalysis

Indexed keywords

BORONIC ACID DERIVATIVE; NAPHTHYL GROUP; RHODIUM;

EID: 11144315424     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.05.031     Document Type: Erratum
Times cited : (17)

References (34)
  • 31
    • 11144268515 scopus 로고    scopus 로고
    • note
    • 2 (244 mg, 2.0 mmol) was added 1,4-dioxane (1.0 mL) and the solution was flushed with argon. After the reaction mixture was stirred at room temperature for 15 min, water (0.1 mL) was added and followed by addition of 2-cyclohexenone (39 mg, 0.40 mmol). The resulting mixture was then stirred at 100°C for 5 h. Purification of the crude product by column chromatography on silica gel (petroleum ether-AcOEt 15/1) gave 3-phenylcyclohexenone 11aa (69 mg, 99%) as colorless oil with 97% ee


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