Radical-mediated annulation reactions. A versatile strategy for the preparation of a series of carbocycles

Organic Letters

Volumn 3, Issue 23, 2001, Pages 3679-3681

  Sibi, Mukund P ^a   Chen, Jianxie ^a   Rheault, Tara R ^a  

^a NORTH DAKOTA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO COMPOUND; FREE RADICAL; HYDROCARBON; ORGANOTIN COMPOUND;

ARTICLE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

BICYCLO COMPOUNDS; FREE RADICALS; HYDROCARBONS, CYCLIC; ORGANOTIN COMPOUNDS; STEREOISOMERISM;

EID: 0035891647     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016597k     Document Type: Article

References (45)

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40. For experimental details, see Supporting Information.
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45. We have not established the stereochemistry of the newly formed center. However, on the basis of our previous work we predict that allyl trapping should occur from a face opposite to the oxazolidinone 4-substituent resulting in the (R)-configuration.