- Intramolecular Cycloadditions: Synthesis of 1-Methylene-2,3,3a,4,5,9b-hexahydro-1H-benzindenes and an unsuccessful approach to Ergot Alkaloids
-
1-(1-Hydroxy-2-trimethylsilylmethylprop-2-enyl)-2-(4-substituted-but-3-enyl)-4-methoxybenzenes, prepared by a short synthesis, underwent intramolecular cycloadditions to produce the title indenes.An analogous intramolecular cycloaddition was attempte
- Collins, Michael P.,Drew, Michael G. B.,Mann, John,Finch, Harry
-
p. 3211 - 3218
(2007/10/02)
-
- Intramolecular (3+2) Cycloadditions
-
1-(1-Hydroxy-2-trimethylsilylmethylprop-2-enyl)-2-(4-methoxybut-3-enyl)-4-methoxybenzene, prepared by a short synthesis, underwent (3+2) cycloaddition to form predominantly the cis-fused tricycle 3,7-dimethoxy-1-methylene-2,3,3a,4,5,9b-hexahydro-1H-benze
- Collins, Michael P.,Mann, John,Capps, Nigel,Finch, Harry
-
p. 239 - 240
(2007/10/02)
-