Regioselective hydroformylation of allylic alcohols

Organic Letters

Volumn 13, Issue 10, 2011, Pages 2686-2689

  Lightburn, Thomas E ^a   De Paolis, Omar A ^a   Cheng, Ka H ^a   Tan, Kian L ^a  

^a BOSTON COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE; ALKENE; ALLYL ALCOHOL; PROPANOL;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; COMBINATORIAL CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALCOHOLS; ALDEHYDES; ALKENES; CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; MOLECULAR STRUCTURE; PROPANOLS; STEREOISOMERISM;

EID: 79956129912     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200782d     Document Type: Article

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61. 13C NMR show that the products are nonidentical (see Supporting Information for details). Based on a syn addition of hydrogen and CO the E -olefin will form the anti product and the Z -olefin will form the syn product.