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RING-OPENING OF BICYCLO[N.1.0]ALKANONES TO 2-CYCLOALKANONE-1,3-DIYLS - WHY DOES OXYALLYL DIRADICAL FORMATION REQUIRE LESS ENERGY FROM BICYCLO[3.1.0]HEXAN-6-ONES THAN FROM BICYCLO[1.1.0]BUTAN-2-ONES
Authors: HROVAT DA RAUK A SORENSEN TS POWELL HK BORDEN WT
Citation: Da. Hrovat et al., RING-OPENING OF BICYCLO[N.1.0]ALKANONES TO 2-CYCLOALKANONE-1,3-DIYLS - WHY DOES OXYALLYL DIRADICAL FORMATION REQUIRE LESS ENERGY FROM BICYCLO[3.1.0]HEXAN-6-ONES THAN FROM BICYCLO[1.1.0]BUTAN-2-ONES, Journal of the American Chemical Society, 118(17), 1996, pp. 4159-4166
CASSCF AND CASPT2N CALCULATIONS PREDICT SINGLET CYCLOPENTAN-2-ONE-1,3-DIYL IS STABLE TOWARD CLOSURE TO BICYCLO[2.1.0]PENTAN-5-ONE
Authors: POWELL HK BORDEN WT
Citation: Hk. Powell et Wt. Borden, CASSCF AND CASPT2N CALCULATIONS PREDICT SINGLET CYCLOPENTAN-2-ONE-1,3-DIYL IS STABLE TOWARD CLOSURE TO BICYCLO[2.1.0]PENTAN-5-ONE, Journal of organic chemistry, 60(9), 1995, pp. 2654-2655
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