Synthesis of a potent (+/-)-4-(2-hydroxyphenyl) analogue of the acromelic acids by dearomatising cyclisation of a lithiated N-p-methoxybenzyl-4-methoxy-l-naphthamide

Dearomatising anionic cyclisation of N-cumyl-N-p-methoxybenzyl-4-methoxy-1- naphthamide 8 diastereoselectively generates a pyrrolidinone-fused tetralon e 12 which may be transformed in seven steps to the racemic form of a known non-natural member of the aryl kainoid family 4 having potent biological a ctivity. Key steps of the synthesis are ruthenium-catalysed oxidation of th e Ci-p-methoxybenzyl ring of 12 to a carboxylic acid and Baeyer-Villiger cl eavage of the tetralone to a lactone whose hydrolysis reveals the two-carbo n substituent at C3 and the 2-hydroxyphenyl substituent at C4. Selective re duction of the lactam yields the kainoid 4. Control of epimerisation at the C-4 centre during the lactone hydrolysis leads to either the (active) 3,4- cis or the (inactive) 3,4-trans epimers of the target. (C) 2001 Elsevier Sc ience Ltd. All rights reserved.