Four hydroxyls are better than two. the use of a chiral lithium salt of 3,3′-bis-methanol-2,2′-binaphthol as a multifunctional catalyst of enantioselective Michael addition reactions

Tetrahedron Asymmetry

Volumn 22, Issue 2, 2011, Pages 167-172

  Belokon, Yuri N ^a   Gugkaeva, Zalina T ^a   Maleev, Victor I ^a   Moskalenko, Margarita A ^a   Tsaloev, Alan T ^a   Khrustalev, Victor N ^a   Hakobyan, Karine V ^b  

^a A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

^b YEREVAN STATE UNIVERSITY   (Armenia)

Author keywords

[No Author keywords available]

Indexed keywords

2 NAPHTHOL; 3,3' BIS METHANOL 2,2' BINAPHTHOL; 3,3' BIS[BIS(PHENYL)HYDROXYMETHYL] 2,2' DIHYDROXY DINAPHTHALENE 1,1'; CARBON; CYCLOHEX 2 ENONE; CYCLOHEXANE DERIVATIVE; HYDROXYL GROUP; LITHIUM SALT; NITROGEN; NITROSTYRENE; STYRENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; MICHAEL ADDITION; PERFORMANCE; PRIORITY JOURNAL; ROOM TEMPERATURE; SOLVATE;

EID: 79952484960     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.12.003     Document Type: Article

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