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Volumn 75, Issue 24, 2010, Pages 8416-8421

6-membered pseudocyclic IBX acids: Syntheses, X-ray structural characterizations, and oxidation reactivities in common organic solvents

Author keywords

[No Author keywords available]

Indexed keywords

BENZYLIC CARBON; CARBONYL COMPOUNDS; CLOSE PACKING OF MOLECULES; ENHANCED REACTIVITY; OXIDATION REACTIVITY; STERICS; STRUCTURAL CHARACTERIZATION; X RAY CRYSTAL STRUCTURES;

EID: 78650356374     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101639j     Document Type: Article
Times cited : (52)

References (55)
  • 53
    • 78650348416 scopus 로고    scopus 로고
    • The reduction product, i.e., I(III) species, failed to oxidize the alcohols. Further, 0.55 equiv of the IBX acid (1PC / 2PC) was found to be sufficient for complete conversion of a sulfide such as methyl phenyl sulfide to the corresponding sulfoxide in the presence of TFA, cf. SI. These two considerations preclude the possibility of disproportionation of I(III) species to I(V) and I(I), and hence as the origin of I(I) species in sulfide oxidations
    • The reduction product, i.e., I(III) species, failed to oxidize the alcohols. Further, 0.55 equiv of the IBX acid (1PC / 2PC) was found to be sufficient for complete conversion of a sulfide such as methyl phenyl sulfide to the corresponding sulfoxide in the presence of TFA, cf. SI. These two considerations preclude the possibility of disproportionation of I(III) species to I(V) and I(I), and hence as the origin of I(I) species in sulfide oxidations.


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