1996
DOI: 10.1021/cr910109c
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Synthetic Aspects of the Di-π-methane Rearrangement

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Cited by 213 publications
(145 citation statements)
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“…[178] Beide Umlagerungen spielen in der Naturstoffsynthese eine weitaus weniger wichtige Rolle als die Oxadi-p-Methanumlagerung. Die Di-p-Methanumlagerung verläuft typischerweise als Singulettprozess, während die Azadi-p-Methanumlagerung sensibilisiert durchgeführt wird.…”
Section: Oxadi-p-methanumlagerungenunclassified
“…[178] Beide Umlagerungen spielen in der Naturstoffsynthese eine weitaus weniger wichtige Rolle als die Oxadi-p-Methanumlagerung. Die Di-p-Methanumlagerung verläuft typischerweise als Singulettprozess, während die Azadi-p-Methanumlagerung sensibilisiert durchgeführt wird.…”
Section: Oxadi-p-methanumlagerungenunclassified
“…An optimization study showed that a ketone in the 2-position of the pyrrole was essential to enable lactam formation (Table 3, entries [1][2][3][4][5] and that a second ketone was actually deleterious to the process (entry 6). Although yields averaged around 50%, this in itself is quite remarkable as intense, high energy 254 nm UV light is used and the successful formation of 22 relies on 3-successive and independent photon mediated events.…”
Section: Scheme 4 Mechanism Of Tricyclic Imine Formationmentioning
confidence: 99%
“…Against this backdrop we wished to explore whether functional groups (R 2 /R 3 ) on the butenyl side chain of pyrrole 4 would influence the outcome of this complex photochemical sequence and lead to single diastereomers of sp 3 -rich aziridines as reactive scaffolds 9 for use in drug discovery. Initially we focused on synthesizing a range of 2-substituted pyrroles (R 1 = CO-Aux) bearing common chiral auxiliaries such as (+)-menthol, Evans' auxiliary, camphor sultam, borneol, and various chiral amines.…”
mentioning
confidence: 99%
“…We later learned that light was responsible for the spectral changes and brief (15 min) irradiation of the sample with a sun lamp converted 47 to a new species which was identified as dicorannulenobullvalene 48 [39]. This photochemical barrelene-semibullvalene conversion, known since 1966 [40], represents a sub-class of the di-p-methane rearrangement [41]. However, the conversion of 47 to 48 is, as far as we are aware, the first reported example induced by visible light since all previous conversions were achieved under UV irradiation.…”
Section: Large Systems With Corannulene Fragmentsmentioning
confidence: 99%