Ene reaction of singlet oxygen, triazolinedione, and nitrosoarene with chiral deuterium-labeled allylic alcohols: The interdependence of diastereoselectivity and regioselectivity discloses mechanistic insights into the hydroxy-group directivity

Journal of the American Chemical Society

Volumn 124, Issue 48, 2002, Pages 14403-14409

  Adam, Waldemar ^a   Bottke, Nils ^a   Krebs, Oliver ^a   Lykakis, Ioannis ^b   Orfanopoulos, Michael ^b   Stratakis, Manolis ^b  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY OF CRETE   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; HYDROGEN BONDS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS;

REGIOSELECTIVITY;

AROMATIC COMPOUNDS;

ALLYL ALCOHOL; DEUTERIUM; HYDROXYL GROUP; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SINGLET OXYGEN; TRIAZOLINE DERIVATIVE;

ARTICLE; CHIRALITY; DIASTEREOISOMER; HYDROGEN BOND; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 0037021527     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja027800p     Document Type: Article

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