Chelation control in the [3+3] annulation reaction of alkoxy-substituted 1,1-diacylcyclopropanes with 1,3-bis(trimethylsilyloxy)-1,3-butadienes
摘要:
Functionalized arenes were prepared by chelation-controlled '[3+3] cyclization/homo-Michael' reactions of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with benzyloxy-or methoxy-substituted 1,1-diacylcyclopropanes. (c) 2008 Elsevier Ltd. All rights reserved.
6-(Pyridyl)salicylates were regioselectively prepared by formal [3+3] cyclization of 1,3-bis(silylenolethers) with 3-(pyridyl)-3-silyloxy-2-en-1-ones. These reactions represent what are, to the best of our knowledge, the first [3+3] cyclizations of 1,3-bis(silylenolethers) with heterocyclic substrates.
Synthesis of 3-aryl-3,4-dihydroisocoumarins by regioselective domino ‘[3+3] cyclization/lactonization’ reactions of 1,3-bis-(silyloxy)-1,3-butadienes with 1-hydroxy-5-silyloxy-4-en-3-ones
The [3+3] cyclization of 1,3-bis(silyloxy)-1,3-butadienes with 1-hydroxy-5-silyloxy-4-en-3-ones afforded 6-(2-aryl-2-chloroethyl)salicylates, which were transformed into 3-aryl-3,4-dihydroisocoumarins by silica gel-mediated lactonization.