938082-20-3Relevant articles and documents
Diastereoselective intramolecular photochemical [2 + 2] cycloaddition reactions of tethered L-(+)-valinol derived tetrahydrophthalimides
Booker-Milburn, Kevin I.,Gulten, Sirin,Sharpe, Andrew
, p. 1385 - 1386 (1997)
Intramolecular photochemical [2 + 2] cycloaddition of allyl alcohol linked to amino acid derived 3,4,5,6-tetrahydrophthalimides, either via a carbonate or silicon tether, gives the corresponding cyclobutanes in excellent yield with diastereoselectivities
Use of temporary tethers in the intramolecular [2+2] photocycloaddition reactions of tetrahydrophthalimide derivatives: a new approach to complex tricyclic lactones
Gülten, ?irin,Sharpe, Andrew,Baker, James R.,Booker-Milburn, Kevin I.
, p. 3659 - 3671 (2007/10/03)
The intramolecular [2+2] photocycloaddition reactions of a series of alkenols tethered to ethanolamine, l-(+)-valinol and R-(-)-2-phenylglycinol derived 3,4,5,6-tetrahydrophthalimides via a carbonate or silicon linkage have been examined. These [2+2] phot