PHOTOINDUCED ELECTRON-TRANSFER REACTION OF CYCLOPROPANONE ACETALS WITH ARYLMETHYL METHANESULFONATE - GENERATION OF BETA-KETO RADICAL SPECIES AND APPLICATION TO C-C BOND FORMATION
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作者:
ABE, M
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KYOTO INST TECHNOL,DEPT CHEM & MAT TECHNOL,SAKYO KU,KYOTO 606,JAPANKYOTO INST TECHNOL,DEPT CHEM & MAT TECHNOL,SAKYO KU,KYOTO 606,JAPAN
ABE, M
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OKU, A
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KYOTO INST TECHNOL,DEPT CHEM & MAT TECHNOL,SAKYO KU,KYOTO 606,JAPANKYOTO INST TECHNOL,DEPT CHEM & MAT TECHNOL,SAKYO KU,KYOTO 606,JAPAN
OKU, A
[1
]
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[1] KYOTO INST TECHNOL,DEPT CHEM & MAT TECHNOL,SAKYO KU,KYOTO 606,JAPAN
The photoinduced electron transfer reaction of the cyclopropanone acetals 1 with arylmethyl methanesulfonates 4 or 10 as electron accepters was found to generate a transient pair of radicals, the beta-keto radical 3 and the arylmethyl radical, which underwent a novel carbon-carbon bond formation reaction at the sterically hindered beta-position of the esters.