Showing papers by "Keiji Maruoka published in 1982"

TL;DR: In this paper, the Beckman rearrangement-alkylation reaction promoted by organoaluminum reagents and a new stereoselective reduction of imino functional group were used to synthesize solenopsin A and B.

TL;DR: The Beckmann rearrangement of oxime sulfonates by Grignard reagents provides an efficient and general entry to α-alkyl- and α,α-dialkylamines in good yields.

TL;DR: In this article, the intramolecular prenyltransfer reaction is accomplished by the rearrangement of allyl ethers with (2,6-di- tert -butyl-4-methylphenoxy)methylaluminum trifluoromethanesulfonate.