Regiocontrolled rearrangement of isobenzofurans

Organic Letters

Volumn 13, Issue 8, 2011, Pages 2086-2089

  Egan, Ben A ^a   Paradowski, Michael ^b   Thomas, Lynne H ^c   Marquez, Rodolfo ^a  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b PFIZER GLOBAL RESEARCH AND DEVELOPMENT   (United Kingdom)

^c University of Bath Claverton Down   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOFURAN DERIVATIVE;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

ALKYLATION; BENZOFURANS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 79955374707     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200498k     Document Type: Article

References (12)

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10. The atomic coordinates for 23A, 23B, and 48B (CCDC deposition nos. CCDC809799, CCDC809800, and CCDC813670) are available upon request from the Cambridge Crystallographic Centre, University Chemical Laboratory, Lensfield Road, Cambridge, CB2 1EW, U.K. The crystallographic numbering system differs from that used in the text; therefore, any request should be accompanied by the full literature citation of this paper.
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12. Each enantiomeric alcoholwas obtained in 49%yield and 99%ee.