Stereoselectivity of the Honda-Reformatsky reaction in reactions with ethyl bromodifluoroacetate with α-oxygenated sulfinylimines

Journal of Organic Chemistry

Volumn 79, Issue 9, 2014, Pages 4186-4195

  Fontenelle, Clément Q ^a   Conroy, Matthew ^a   Light, Mark ^a   Poisson, Thomas ^b   Pannecoucke, Xavier ^b   Linclau, Bruno ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^b UNIVERSITÉ DE ROUEN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

FUNCTIONAL GROUPS;

DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVITIES; REFORMATSKY REACTION; SULFINYL GROUP;

STEREOSELECTIVITY;

ACETIC ACID ETHYL ESTER; ALDEHYDE; BROMODIFLUOROACETIC ACID ETHYL ESTER; IMINE; SULFINYLIMINE; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; ENANTIOMER; HONDA REFORMATSKY REACTION; OXYGENATION; REACTION OPTIMIZATION; REFORMATSKY REACTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 84899867949     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo500396p     Document Type: Article

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