Facile synthesis of enantiopure 1,1′-spirobiindane-7,7′-diol and its 4,4′-derivatives: Application in enantioselective addition of diethylzinc to aromatic aldehydes

Synthesis

Volumn , Issue 17, 2004, Pages 2805-2808

  Li, Zhian ^a   Liang, Xinmiao ^a   Wan, Boshun ^a   Wu, Fan ^a  

^a NONE

Author keywords

Aldehydes; Alkylations; Enantiomeric resolution; Protecting groups; Spiro compounds; Stereoselectivity

Indexed keywords

ALDEHYDES; CATALYSTS; CORRELATION METHODS; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); ZINC;

ABSOLUTE CONFIGURATIONS; CHEMICAL CORRELATION; ENANTIOSELECTIVITIES; FACILE SYNTHESIS;

ALCOHOLS;

1,1' SPIROBIINDANE 7,7' DIOL; 4,4' DIBROMO 1,1' SPIROBIINDANE 7,7' DIYL BISMENTHYL CARBONATE; 4,4' DIIODO 1,1' SPIROBIINDANE 7,7' DIOL; 4,4' DIMETHYL 1,1' SPIROBIINDANE 7,7' DIOL; ALDEHYDE DERIVATIVE; AROMATIC COMPOUND; BISMENTHYL CARBONATE; BROMINE DERIVATIVE; CARBONIC ACID DERIVATIVE; DIETHYLZINC; INDAN DERIVATIVE; IODINE DERIVATIVE; LITHIUM DERIVATIVE; METHYL GROUP; OXIDE; SPIRO COMPOUND; TITANIUM; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CATALYST; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; DISSOCIATION; ENANTIOMER; ENANTIOSELECTIVITY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; REPRODUCIBILITY; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS; TECHNIQUE;

EID: 10644273572     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-831238     Document Type: Article

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