2,4-Cyclohexadien-1-ones in organic synthesis. Intramolecular Diels-Alder reactivity and the oxa-di-.pi.-methane photorearrangement of Diels-Alder adducts
2,4-Cyclohexadien-1-ones in organic synthesis. Intramolecular Diels-Alder reactivity and the oxa-di-.pi.-methane photorearrangement of Diels-Alder adducts
2,5-Cyclohexadien-1-one to bicyclo[3.1.0]hexenone photorearrangement. Development of the reaction for use in organic synthesis
作者:Arthur G. Schultz、Frank P. Lavieri、Mark Macielag、Mark Plummer
DOI:10.1021/ja00247a027
日期:1987.6
Le mecanisme le plus plausible fait intervenir un zwitterion de preference a un biradical organique
Le mecanisme le plus plausible fait intervenir un zwitterion de preferred a un biradicalorganique
SCHULTZ, A. G.;LAVIERI, F. P.;SNEAD, T. E., J. ORG. CHEM., 1985, 50, N 17, 3086-3091
作者:SCHULTZ, A. G.、LAVIERI, F. P.、SNEAD, T. E.
DOI:——
日期:——
SCHULTZ, A. G.;LAVIERI, F. P.;MACIELAG, M.;PLUMMER, M., J. AMER. CHEM. SOC., 109,(1987) N 13, 3991-4000
作者:SCHULTZ, A. G.、LAVIERI, F. P.、MACIELAG, M.、PLUMMER, M.
DOI:——
日期:——
2,4-Cyclohexadien-1-ones in organic synthesis. Intramolecular Diels-Alder reactivity and the oxa-di-.pi.-methane photorearrangement of Diels-Alder adducts
作者:Arthur G. Schultz、Frank P. Lavieri、Thomas E. Snead