Transannular Diels-Alder approach to the synthesis of momilactone A
摘要:
The application of the transannular Diels-Alder strategy on macrocyclic trienes having the trans-trans-cis olefin geometry led to trans-syn-trans tricycles which are advanced intermediates for the synthesis of natural products like Momilactone A. (C) 1999 Elsevier Science Ltd. All rights reserved.
The first total synthesis of (+/-)-momilactone A was accomplished using a highly diastereoselective transannular Diels-Alder reaction on a trans-trans-cis macrocyclic triene.