Formation of an aromatic indenide anion in a bridge-annelated [2.2]metacyclophanene: A novel and stereoselective nucleophilic addition to an acenaphthylene derivative

Tetrahedron Letters

Volumn 44, Issue 1, 2003, Pages 23-26

  Chen, Pu ^a   Lai, Yee Hing ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

Acenaphthyleno metacyclophanene; Aromatization; Geometric strain; Indenide anion; Nucleophilic addition

Indexed keywords

ALKADIENE; ANION; BRIDGED COMPOUND; CYCLOPHANE DERIVATIVE; INDENE DERIVATIVE; LITHIUM DERIVATIVE; METACYCLOPHANE DERIVATIVE; METHYL IODIDE; NAPHTHYL GROUP; PYRENE DERIVATIVE; SULFONIUM DERIVATIVE;

ANNELATION; ARTICLE; CHEMICAL REACTION; ELIMINATION REACTION; GEOMETRY; HOFMANN ELIMINATION; ISOMERISM; METHYLATION; STEREOCHEMISTRY; SYNTHESIS; WITTIG REARRANGEMENT;

EID: 0037213613     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02517-0     Document Type: Article

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