The power of solvent in altering the course of photorearrangements

. 2011 Feb 18 ; 13 (4) : 644-7. [epub] 20110114

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid21235252

Grantová podpora
R01 GM072910-04 NIGMS NIH HHS - United States
R01 GM72910 NIGMS NIH HHS - United States
R01 GM072910 NIGMS NIH HHS - United States
GM069663 NIGMS NIH HHS - United States
P50 GM069663 NIGMS NIH HHS - United States

A clean bifurcation between two important photochemical reactions through competition of a triplet state Type II H-abstraction reaction with a photo-Favorskii rearrangement for (o/p)-hydroxy-o-methylphenacyl esters that depends on the water content of the solvent has been established. The switch from the anhydrous Type II pathway that yields indanones to the aqueous-dependent pathway producing benzofuranones occurs abruptly at low water concentrations (~8%). The surprisingly clean yields suggest that such reactions are synthetically promising.

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